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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69956생성일: 2026년 10월 24일

1,2-Dichloroethane → Tert-butyl 6-(3-(3-amino-6-bromopicolinamido)pyridine-4-yl)-2-(trifluoromethyl)pyrimidin-4-ylcarbamate

https://huagongshe.com/ko/reaction/69956

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물HOAtHCID 181649—
반응물3-Amino-6-bromopicolinic acidHCID 45480452—
반응물Tert-butyl 6-(3-aminopyridin-4-yl)-2-(trifluoromethyl)pyrimidin-4-ylcarbamateHCID 69047673—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 6-(3-(3-amino-6-bromopicolinamido)pyridine-4-yl)-2-(trifluoromethyl)pyrimidin-4-ylcarbamateHCID 8666920181%

반응 조건

온도50 °C

반응 단계

A solution of tert-butyl 6-(3-aminopyridin-4-yl)-2-(trifluoro-methyl)pyrimidin-4-ylcarbamate (1.0 equiv.), 3-amino-6-bromopicolinic acid (1.0 equiv.), HOAt (1.0 equiv.), and EDC (1.0 equiv.) in DMF at a concentration of (0.2 M) was stirred for 3 hrs then heated to 50° C. overnight (homogeneous solution). Water was added to the reaction and the precipitate was filtered. The solid was further purified via SiO2 column chromatography eluting with DCM/MeOH (10%) to yield a brown solid as the desired product (81%). LCMS (m/z): 554.1/556.1 (MH+); LC Rt=3.77 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822497B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d2aa46996bb04bed9468f82fb3d01a4a
출처 메모uspto-grants-2014_09