돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69880생성일: 2026년 10월 23일

1,2-Dichloroethane → Tert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate

https://huagongshe.com/ko/reaction/69880

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물HOAtHCID 181649—
반응물3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
반응물Tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamateHCID 67130164—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamateHCID 86669179—

반응 단계

A solution containing 1 eq each of tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate, 3-amino-6-bromopyrazine-2-carboxylic acid, HOAT and EDC in DMF, at a concentration of 0.5 M, was stirred for 60 hours. The solution was diluted with EtOAc and was washed with H2O (4×), NaCl(sat.), was dried over MgSO4, was filtered and the volatiles were removed in vacuo. After purification by silica gel chromatography (EtOAc eluant), tert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate was obtained (78%). LCMS (m/z): 492.2 (MH+); LC Rt=2.68 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822497B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9592b42608d044f0b3167cbee937b637
출처 메모uspto-grants-2014_09