돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1410067생성일: 2026년 10월 26일

Diisopropylethylamine → N-(3-((1R,5S)-8-oxa-3-azabicyclo[3.2.1]octan-3-yl)phenyl)-5-chlorothiazolo[5,4-d]pyrimidin-7-amine

https://huagongshe.com/reaction/1410067

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5,7-Dichlorothiazolo(5,4-d)pyrimidineHCID 609639—
반응물3-((1R,5S)-8-oxa-3-azabicyclo[3.2.1]octan-3-yl)anilineHCID 68379258—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물N-(3-((1R,5S)-8-oxa-3-azabicyclo[3.2.1]octan-3-yl)phenyl)-5-chlorothiazolo[5,4-d]pyrimidin-7-amineHCID 8667178686%

반응 조건

온도30 °C

반응 단계

The mixture of 3-((1R,5S)-8-oxa-3-azabicyclo[3.2.1]octan-3-yl)aniline (0.061 g, 0.3 mmol), 5,7-dichlorothiazolo[5,4-d]pyrimidine (0.061 g, 0.3 mmol) and DIPEA (0.046 g, 0.36 mmol) in DMSO (10 mL) was heated to 30° C. for 2 h. Then it was diluted with water and extracted with ethyl acetate (3×10 mL), the organics were dried and concentrated. The residue was purified by column chromatography (silica gel, 200˜300 mesh, eluting with MeOH:DCM=1:80) to afford N-(3-((1R,5S)-8-oxa-3-azabicyclo[3.2.1]octan-3-yl)phenyl)-5-chlorothiazolo[5,4-d]pyrimidin-7-amine (0.095 g, 86%) as a yellow solid. LC-MS: 374 [M+H]+, tR=1.66 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921383B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-26f0d20983bd490c9364c0ed844e1b01
출처 메모uspto-grants-2014_12