【结 构 式】 |
【分子编号】19955 【品名】1-trityl-4-piperidinylamine; 1-trityl-4-piperidinamine 【CA登记号】 |
【 分 子 式 】C24H26N2 【 分 子 量 】342.48392 【元素组成】C 84.17% H 7.65% N 8.18% |
合成路线1
该中间体在本合成路线中的序号:(II)The condensation of 4-amino-5-chloro-2-methoxybenzoic acid (I) with 4-amino-1-(triphenylmethyl)piperidine (II) by means of ethyl chloroformate and triethylamine in THF gives the corresponding amide (III), which is deprotected with HCl in actone yielding 4-amino-5-chloro-2-methoxy-N-(4-piperidyl)benzamide (IV). The condensation of (IV) with ethyl bromoacetate (V) by means of K2CO3 in DMF affords the substituted acetate (VI), which is finally saponified with NaOH in methanol.
【1】 Ito, Y.; Kato, H.; Yasuda, S.; Iwasaki, N.; Nishino, H.; Takeshita, M. (Hokuriku Seiyaku Co., Ltd.); Benzamide deriv.. EP 0640601; US 5395832; US 5500422; WO 9214705 . |
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) | 12419 | 4-Amino-5-chloro-2-methoxybenzoic acid | 7206-70-4 | C8H8ClNO3 | 详情 | 详情 |
(II) | 19955 | 1-trityl-4-piperidinylamine; 1-trityl-4-piperidinamine | C24H26N2 | 详情 | 详情 | |
(III) | 19956 | 4-amino-5-chloro-2-methoxy-N-(1-trityl-4-piperidinyl)benzamide | C32H32ClN3O2 | 详情 | 详情 | |
(IV) | 19957 | 4-amino-5-chloro-2-methoxy-N-(4-piperidinyl)benzamide | C13H18ClN3O2 | 详情 | 详情 | |
(V) | 16640 | Ethyl 2-bromoacetate; Ethyl bromoacetate | 105-36-2 | C4H7BrO2 | 详情 | 详情 |
(VI) | 19959 | ethyl 2-[4-[(4-amino-5-chloro-2-methoxybenzoyl)amino]-1-piperidinyl]acetate | C17H24ClN3O4 | 详情 | 详情 |
合成路线2
该中间体在本合成路线中的序号:(III)4-Amino-5-chloro-2-methoxybenzoic acid (I) was converted to the mixed anhydride (II) upon treatment with ethyl chloroformate and Et3N. Subsequent coupling of (II) with 4-amino-1-tritylpiperidine (III) afforded amide (IV). The trityl group of (IV) was then removed by acidic treatment to give piperidine (V). Finally, alkylation of (V) with butyl bromoacetate (VI) furnished the title compound.
【1】 Ito, Y.; Kato, H.; Yasuda, S.; Iwasaki, N.; Nishino, H.; Takeshita, M. (Hokuriku Seiyaku Co., Ltd.); Benzamide deriv.. EP 0640601; US 5395832; US 5500422; WO 9214705 . |
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) | 12419 | 4-Amino-5-chloro-2-methoxybenzoic acid | 7206-70-4 | C8H8ClNO3 | 详情 | 详情 |
(II) | 29299 | 4-Amino-5-chloro-2-methoxybenzoic acid methoxycarbonyl anhydride | C10H10ClNO5 | 详情 | 详情 | |
(III) | 19955 | 1-trityl-4-piperidinylamine; 1-trityl-4-piperidinamine | C24H26N2 | 详情 | 详情 | |
(IV) | 19956 | 4-amino-5-chloro-2-methoxy-N-(1-trityl-4-piperidinyl)benzamide | C32H32ClN3O2 | 详情 | 详情 | |
(V) | 19957 | 4-amino-5-chloro-2-methoxy-N-(4-piperidinyl)benzamide | C13H18ClN3O2 | 详情 | 详情 | |
(VI) | 29300 | butyl 2-bromoacetate | C32H32ClN3O2 | 详情 | 详情 |