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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1986255생성일: 2026년 10월 24일

tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate → 2-[5-Chloro-2-(2-piperazin-1-ylethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride

https://huagongshe.com/ko/reaction/1986255

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 1514400—
반응물[4-(Benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochlorideHCID 68855962—
반응물2-(2,5-Dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamideHCID 86625351—
생성물2-[5-Chloro-2-(2-piperazin-1-ylethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochlorideHCID 68857404—

반응 단계

Using the method of [4-(benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochloride, the title compound is synthesized from 2-(2,5-dichloro-pyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamide and 4-(2-amino-ethyl)-piperazine-1-carboxylic acid tert-butyl ester and isolated as a yellow solid (80% yield). ES+(m/z) 457 (35Cl) and 459 (37Cl) [M(free base)+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07547691B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-54a0a2b717e248feb44bd2c85c249ed5
출처 메모uspto-grants-2009_06