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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19633생성일: 2026년 10월 24일

Diisopropylethylamine → 5,6,7,8-tetrahydro-N-(4-(trifluoromethylsulfonyl)phenyl)pyrido[4,3-d]pyrimidin-4-amine

https://huagongshe.com/ko/reaction/19633

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-Chloroethyl chloroformateHCID 521305—
반응물6-Benzyl-5,6,7,8-tetrahydro-N-(4-(trifluoromethylsulfonyl)phenyl)pyrido[4,3-d]pyrimidin-4-amineHCID 59346557—
용매ChloroformHCID 6212—
생성물5,6,7,8-tetrahydro-N-(4-(trifluoromethylsulfonyl)phenyl)pyrido[4,3-d]pyrimidin-4-amineHCID 5934645483%

반응 단계

6-Benzyl-5,6,7,8-tetrahydro-N-(4-(trifluoromethylsulfonyl)phenyl)pyrido[4,3-d]pyrimidin-4-amine (270 mg, 0.55 mmol) was dissolved in anhydrous chloroform (10 mL) and 1-chloroethylchloroformate was added (0.18 mL, 1.65 mmol). After stirring for 30 min, N,N-diisopropylethylamine was added (0.24 mL, 1.65 mmol) and the mixture was stirred for an additional 2 h. The chloroform was removed under vacuum and 30 ml of methanol was added and the mixture was heated for 30 min. Upon reaction completion, the methanol was removed and the residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give the product (163 mg, 83%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745451B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4801c6f6649e49269c71b088f756b648
출처 메모uspto-grants-2010_06