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【结 构 式】

【分子编号】59945

【品名】(E)-3-(dimethylamino)-2-(2-thienylcarbonyl)-2-propenenitrile

【CA登记号】

【 分 子 式 】C10H10N2OS

【 分 子 量 】206.26828

【元素组成】C 58.23% H 4.89% N 13.58% O 7.76% S 15.55%

与该中间体有关的原料药合成路线共 3 条

合成路线1

该中间体在本合成路线中的序号:(IV)

Condensation of 2-acetylthiophene (I) with dimethylformamide dimethylacetal produced enaminone (II), which was subsequently cyclized to the isoxazole (III) upon treatment with hydroxylamine. Further condensation of (III) with dimethylformamide dimethylacetal, with concomitant isoxazole ring opening, gave rise to the enamino nitrile (IV). This was then cyclized with aminoguanidine nitrate (V) under basic conditions to furnish the intermediate aminopyrazole (VI).

2 Tomcufcik, A.S.; Dusza, J.P.; Albright, J.D.; Beer, B. (Wyeth); N-Methyl-N-(-[3-[-2-thienylcarbonyl]-pyrazol-[1,5-alpha]-pyrimidin-7-yl]phenyl)acetamide and compsns. and methods related thereto. US 6399621 .
1 Sorbera, L.A.; Castaner, J.; Martin, L.; Indiplon. Drugs Fut 2003, 28, 8, 739.
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) 24490 1-(2-Thienyl)-1-ethanone; 2-Acetylthiophene 88-15-3 C6H6OS 详情 详情
(II) 59943 (E)-3-(dimethylamino)-1-(2-thienyl)-2-propen-1-one C9H11NOS 详情 详情
(III) 59944 5-(2-thienyl)isoxazole C7H5NOS 详情 详情
(IV) 59945 (E)-3-(dimethylamino)-2-(2-thienylcarbonyl)-2-propenenitrile C10H10N2OS 详情 详情
(V) 10015 1-Hydrazinecarboximidamide; Hydrazinecarboximidamide 79-17-4 CH6N4 详情 详情
(VI) 59946 (3-amino-1H-pyrazol-4-yl)(2-thienyl)methanone C8H7N3OS 详情 详情

合成路线2

该中间体在本合成路线中的序号:(IV)

Reaction of 3-(acetamido)acetophenone (VIII) with iodomethane and NaH gives 3-(N-methylacetamido)acetophenone (XXVIII), which is mixed with 3-oxo-3-(2-thienyl)propionitrile (VII) and treated with dimethylformamide dimethylacetal to yield a mixture of the dimethylaminomethylene derivatives (IV) and (X). This mixture, without isolation, is cyclized with aminoguanidine (V) by treatment first with NaOH in ethanol and then with refluxing AcOH.

1 Sorbera, L.A.; Castaner, J.; Martin, L.; Indiplon. Drugs Fut 2003, 28, 8, 739.
2 Wilcoxen, K.M.; Gross, R.S. (Neurocrine Biosciences Inc.); Synthesis of substd. pyrazolopyrimidines. WO 0110868 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV) 59945 (E)-3-(dimethylamino)-2-(2-thienylcarbonyl)-2-propenenitrile C10H10N2OS 详情 详情
(V) 10015 1-Hydrazinecarboximidamide; Hydrazinecarboximidamide 79-17-4 CH6N4 详情 详情
(VII) 62972 3-oxo-3-(2-thienyl)propanenitrile C7H5NOS 详情 详情
(VIII) 11983 3'-Acetamidoacetophane; m-Acetamidoacetophenone; N-(3-Acetylphenyl)acetamide 7463-31-2 C10H11NO2 详情 详情
(X) 59947 N-{3-[(E)-3-(dimethylamino)-2-propenoyl]phenyl}-N-methylacetamide C14H18N2O2 详情 详情
(XXVIII) 62971 N-(3-acetylphenyl)-N-methylacetamide C11H13NO2 详情 详情

合成路线3

该中间体在本合成路线中的序号:(IV)

The enamino nitrile (IV) can be obtained by condensation of 3-oxo-3-(2-thienyl)propionitrile (VII) with dimethylformamide dimethylacetal in chloroform.

1 Sorbera, L.A.; Castaner, J.; Martin, L.; Indiplon. Drugs Fut 2003, 28, 8, 739.
2 Tomcufcik, A.S.; Dusza, J.P. (Wyeth); (3-Amino-1H-pyrazol-4-yl)(aryl)methanones. EP 0129846; JP 1985013764; US 4900836 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV) 59945 (E)-3-(dimethylamino)-2-(2-thienylcarbonyl)-2-propenenitrile C10H10N2OS 详情 详情
(VII) 62972 3-oxo-3-(2-thienyl)propanenitrile C7H5NOS 详情 详情
Extended Information