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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400956생성일: 2026년 10월 25일

5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine → {1-[5-tert-Butyl-3-(2-chloro-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-yl}-methyl-amine

https://huagongshe.com/reaction/400956

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참여 물질

역할이름HCID투입량
반응물5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 1433953—
반응물3-(Methylamino)pyrrolidineHCID 11788268—
반응물5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683284—
생성물{1-[5-tert-Butyl-3-(2-chloro-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-pyrrolidin-3-yl}-methyl-amineHCID 86683367—

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In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chlorobenzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and N-methylpyrrolidin-3-amine. MS (m/e): 400.3 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741906B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-2913438f858a4330ac50bf0fe7fcbecc
출처 메모uspto-grants-2014_06