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【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%

与该中间体有关的原料药合成路线共 2 条

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
Extended Information