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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400826생성일: 2026년 10월 26일

5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine → 5-tert-Butyl-3-(2-chloro-benzyl)-7-(6-oxa-1-aza-spiro[3.3]hept-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/400826

반응식

참여 물질

역할이름HCID투입량
반응물5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 1433953—
반응물6-Oxa-1-azaspiro[3.3]heptane oxalateHCID 71303992—
반응물5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683284—
생성물5-tert-Butyl-3-(2-chloro-benzyl)-7-(6-oxa-1-aza-spiro[3.3]hept-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71557722—

반응 단계

In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chloro-benzyl)-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 6-oxa-1-azaspiro[3.3]heptane oxalate and isolated as light-yellow gum (12.5 mg, 65%). MS (m/e): 399.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741906B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-57407c8a13904c1891c2673f329c9969
출처 메모uspto-grants-2014_06