돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562167생성일: 2026년 10월 26일

2-Methylbutylamine, (S)- → [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid

https://huagongshe.com/reaction/562167

반응식

참여 물질

역할이름HCID투입량
반응물2-Methylbutylamine, (S)-HCID 2724272—
반응물5-Formyl-2-thiopheneboronic acidHCID 2773430—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-{[(2-methylbutyl)amino]methyl}-2-thienyl)-1H-indole-7-carboxamideHCID 57732791—
생성물[5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acidHCID 66723247—

반응 단계

Following the general procedure of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-{[(2-methylbutyl)amino]methyl}-2-thienyl)-1H-indole-7-carboxamide, (5-formyl-2-thienyl)boronic acid (50 mg, 0.32 mmol), [(2S)-2-methylbutyl]amine (28 mg, 0.32 mmol), and NaCNBH3 (40 mg, 0.64 mmol) were reacted to give 43 mg of crude [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid. The crude [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid was then reacted with 5-bromo-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide (65 mg, 0.157 mmol), K2CO3 (130 mg, 0.942 mmol), and tetrakis(triphenylphosphine)palladium(0) (4 mg, 0.003 mmol) to give 37.6 mg of the title compound (39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063071B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-3dc89a23f295438e9e9689aee189d27a
출처 메모uspto-grants-2011_11