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【结 构 式】 
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【分子编号】25062 【品名】4-methoxybenzyl 3-(chloromethyl)-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 【CA登记号】 |
【 分 子 式 】C41H36ClN5O6S2 【 分 子 量 】794.35164 【元素组成】C 61.99% H 4.57% Cl 4.46% N 8.82% O 12.08% S 8.07% |
合成路线1
该中间体在本合成路线中的序号：(IIIb)The cephalosporin was synthesized following the reaction pathway depicted in Scheme 25490101a: Protected 2-(2-aminothiazol-4-yl)-2-(alkoxy)iminoacetic acid ((Ia-c) was reacted with p-methoxybenzyl 7-amino-3-chloromethyl-cephaslosporonate (II) by a conventional method (POCl3, pyr / CH2Cl2. -5 C) to give the acylated product (IIIa-c). Product (IIIa-c) was then coverted to a phosponium salt (Iva-c) (PPh3, NaI / acetone, r.t.), followed by the reaction (NaHCO3(2N) / CH2Cl2, 0 C - r.t.) with a substituted isoxazole aldehyde (V) to afford the protected final product (Via-c). The aldehyde (V) was prepared by the sequential reduction-oxidation of the 1,3-dipolar cycloaddition product of methyl propiolate and the corresponding aldoxime. Deprotection, sodium salt formation and purification by reverse phase column chromatography (LiChrosorb(R) RP-18, 25% aq. MeOH) followed by frezee drying gave the final product as an amorphous white solid.
| 【1】 Choi, K.I.; Discovery of novel 3-isoxazolylvinylcephalosporins. Drugs Fut 1999, 24, 3, 287. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (Ia) | 25057 | 2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetic acid | C43H33N3O3S | 详情 | 详情 | |
| (Ib) | 25058 | 2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | 64485-90-1 | C25H21N3O3S | 详情 | 详情 |
| (Ic) | 25059 | 2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | C29H27N3O3S | 详情 | 详情 | |
| (IIIa) | 25061 | 4-methoxybenzyl 3-(chloromethyl)-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C59H48ClN5O6S2 | 详情 | 详情 | |
| (IIIb) | 25062 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C41H36ClN5O6S2 | 详情 | 详情 | |
| (IIIc) | 25063 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C45H42ClN5O6S2 | 详情 | 详情 | |
| (IVa) | 25064 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium iodide | C77H63IN5O6PS2 | 详情 | 详情 | |
| (IVb) | 25065 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium iodide | C59H51IN5O6PS2 | 详情 | 详情 | |
| (IVc) | 25066 | [(7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-2-[[(4-methoxybenzyl)oxy]carbonyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl](triphenyl)phosphonium iodide | C63H57IN5O6PS2 | 详情 | 详情 | |
| (VIa) | 25068 | 4-methoxybenzyl 3-[(E)-2-(3-chloro-5-isoxazolyl)ethenyl]-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C63H49ClN6O7S2 | 详情 | 详情 | |
| (VIb) | 25069 | 4-methoxybenzyl 3-[(E)-2-(3-chloro-5-isoxazolyl)ethenyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C45H37ClN6O7S2 | 详情 | 详情 | |
| (VIc) | 25070 | 4-methoxybenzyl 3-[(E)-2-(3-chloro-5-isoxazolyl)ethenyl]-7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C49H43ClN6O7S2 | 详情 | 详情 | |
| (II) | 25060 | 4-methoxybenzyl 3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C16H16ClNO4S | 详情 | 详情 | |
| (V) | 25067 | 3-chloro-5-isoxazolecarbaldehyde | C4H2ClNO2 | 详情 | 详情 |
合成路线2
该中间体在本合成路线中的序号：(IIIb)The cephalosporin was synthesized following the reaction pathway depicted in Scheme 25490201a: Protected 2-(2-aminothiazol-4-yl)-2-(alkoxy)iminoacetic acid ((Ia-c) was reacted with p-methoxybenzyl 7-amino-3-chloromethyl-cephaslosporonate (II) by a conventional method (POCl3, pyr / CH2Cl2. -5 C) to give the acylated product (IIIa-c). Product (IIIa-c) was then coverted to a phosponium salt (Iva-c) (PPh3, NaI / acetone, r.t.), followed by the reaction (NaHCO3(2N) / CH2Cl2, 0 C - r.t.) with a substituted isoxazole aldehyde (V) to afford the protected final product (Via-c). The aldehyde (V) was prepared by the sequential reduction-oxidation of the 1,3-dipolar cycloaddition product of methyl propiolate and the corresponding aldoxime. Deprotection, sodium salt formation and purification by reverse phase column chromatography (LiChrosorb(R) RP-18, 25% aq. MeOH) followed by frezee drying gave the final product as an amorphous white solid.
| 【1】 Choi, K.I.; Discovery of novel 3-isoxazolylvinylcephalosporins. Drugs Fut 1999, 24, 3, 287. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (Ia) | 25057 | 2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetic acid | C43H33N3O3S | 详情 | 详情 | |
| (Ib) | 25058 | 2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | 64485-90-1 | C25H21N3O3S | 详情 | 详情 |
| (Ic) | 25059 | 2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | C29H27N3O3S | 详情 | 详情 | |
| (IIIa) | 25061 | 4-methoxybenzyl 3-(chloromethyl)-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C59H48ClN5O6S2 | 详情 | 详情 | |
| (IIIb) | 25062 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C41H36ClN5O6S2 | 详情 | 详情 | |
| (IIIc) | 25063 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C45H42ClN5O6S2 | 详情 | 详情 | |
| (IVa) | 25064 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium iodide | C77H63IN5O6PS2 | 详情 | 详情 | |
| (IVb) | 25065 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium iodide | C59H51IN5O6PS2 | 详情 | 详情 | |
| (IVc) | 25066 | [(7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-2-[[(4-methoxybenzyl)oxy]carbonyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl](triphenyl)phosphonium iodide | C63H57IN5O6PS2 | 详情 | 详情 | |
| (VIa) | 25072 | 4-methoxybenzyl 3-[(E)-2-(3-methoxy-5-isoxazolyl)ethenyl]-8-oxo-7-([2-[2-(tritylamino)-1,3-thiazol-4-yl]-2-[(trityloxy)imino]acetyl]amino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C64H52N6O8S2 | 详情 | 详情 | |
| (VIb) | 25073 | 4-methoxybenzyl 7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-3-[(E)-2-(3-methoxy-5-isoxazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C46H40N6O8S2 | 详情 | 详情 | |
| (VIc) | 25074 | 4-methoxybenzyl 7-([2-[(cyclopentyloxy)imino]-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-3-[(E)-2-(3-methoxy-5-isoxazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C50H46N6O8S2 | 详情 | 详情 | |
| (II) | 25060 | 4-methoxybenzyl 3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C16H16ClNO4S | 详情 | 详情 | |
| (V) | 25071 | 3-methoxy-5-isoxazolecarbaldehyde | C5H5NO3 | 详情 | 详情 |
合成路线3
该中间体在本合成路线中的序号：(III)Trityl protected 2-(2-aminothiazol-4-yl)-2-(methoxy)iminoacetic acid (I) was coupled to 7-amino-3-(chloromethyl)cephalosporanic acid p-methoxybenzyl ester (II) using POCl3 and pyridine to give amide (III). This was converted to phosphonium salt (IV) upon treatment with triphenylphosphine and NaI. Subsequent Wittig reaction of (IV) with 3-chloroisoxazole-5-carbaldehyde (V) produced the corresponding vinyl isoxazole as a mixture of geometrical isomers, from which the major trans isomer (VI) was separated by flash column chromatography. Finally, deprotection of both trityl and p-methoxybenzyl groups of (VI) by means of trifluoroacetic acid afforded the title compound, which was isolated as the sodium salt.
| 【1】 Cho, Y.S.; Pae, A.N.; Cha, J.H.; Choi, K.I.; Chang, M.H.; Koh, H.Y.; Studies on novel 3-isoxazolylvinylcephalosporins: I. Synthesis and biological activity of 7-[2-(2-aminothiazol-4-yl)-2-(alkoxy)iminoacetamido] derivatives. J Antibiot 1998, 51, 12, 1117. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (I) | 25058 | 2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | 64485-90-1 | C25H21N3O3S | 详情 | 详情 |
| (II) | 26869 | 4-methoxybenzyl 7-amino-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C16H17ClN2O4S | 详情 | 详情 | |
| (III) | 25062 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C41H36ClN5O6S2 | 详情 | 详情 | |
| (IV) | 25065 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium iodide | C59H51IN5O6PS2 | 详情 | 详情 | |
| (V) | 25067 | 3-chloro-5-isoxazolecarbaldehyde | C4H2ClNO2 | 详情 | 详情 | |
| (VI) | 26870 | 4-methoxybenzyl 3-[(E)-2-(3-chloro-5-isoxazolyl)ethenyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C45H37ClN6O7S2 | 详情 | 详情 |
合成路线4
该中间体在本合成路线中的序号：(III)Coupling of carboxylic acid (II) to the 7-aminocephem derivative (I) using POCl3 and pyridine produced the corresponding amide (III). Displacement of the chloro group of (III) with triphenyl phosphine furnished the phosphonium salt (IV), which was subjected to a Wittig reaction with chloroacetaldehyde (V), yielding the Z-propenyl chloride (VI). Subsequent reaction of allyl chloride (VI) with 4-amino-2-mercapto-6-methylpyrimidine (VII) in the presence of NaI produced the E-propenyl sulfide (VIII). The N-trityl group and the p-methoxybenzyl ester of (VIII) were finally cleaved by treatment with trifluoroacetic acid in anisole to furnish the title compound.
| 【1】 Lee, C.-S.; et al.; Synthesis and antibacterial activities of novel C(3)-aminopyrimidinyl substituted cephalosporins. J Antibiot 2000, 53, 11, 1305. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (I) | 26869 | 4-methoxybenzyl 7-amino-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C16H17ClN2O4S | 详情 | 详情 | |
| (II) | 25058 | 2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acid | 64485-90-1 | C25H21N3O3S | 详情 | 详情 |
| (III) | 25062 | 4-methoxybenzyl 3-(chloromethyl)-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C41H36ClN5O6S2 | 详情 | 详情 | |
| (IV) | 47060 | [[2-[[(4-methoxybenzyl)oxy]carbonyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl](triphenyl)phosphonium chloride | C59H51ClN5O6PS2 | 详情 | 详情 | |
| (V) | 47061 | 2-chloroacetaldehyde | 107-20-0 | C2H3ClO | 详情 | 详情 |
| (VI) | 47062 | 4-methoxybenzyl 3-[(Z)-3-chloro-1-propenyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C43H38ClN5O6S2 | 详情 | 详情 | |
| (VII) | 47063 | 2-amino-6-methyl-4-pyrimidinethiol; 2-amino-6-methyl-4-pyrimidinylhydrosulfide | C5H7N3S | 详情 | 详情 | |
| (VIII) | 47064 | 4-methoxybenzyl 3-[(E)-3-[(2-amino-6-methyl-4-pyrimidinyl)sulfanyl]-1-propenyl]-7-([2-(methoxyimino)-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | C48H44N8O6S3 | 详情 | 详情 |