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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2205616생성일: 2026년 10월 27일

Sodium borohydride → 1-(6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)propan-1-amine

https://huagongshe.com/reaction/2205616

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine-5-carbonitrileHCID 86707963—
반응물HCID 178418443HCID 178418443—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)propan-1-amineHCID 11820775881%

반응 단계

Ethylmagnesium bromide (4.18 mL, 12.54 mmol) was added to a stirred solution of 6-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine-5-carbonitrile (740 mg, 3.13 mmol) in THF (16 mL) at room temperature. The mixture was stirred for one hour at room temperature and then quenched with methanol (5 mL). Sodium borohydride (237 mg, 6.27 mmol) was added. The reaction mixture was stirred for one hour, quenched with 1N HCl (1.5 mL) and stirred for 20 minutes. Next, the mixture was basified with saturated aqueous sodium bicarbonate and extracted with ethyl acetate (2×). The organic layer was dried over anhydrous magnesium sulfate and concentrated to give the title compound as a tan oil (680 mg, 81%). ESI-MS m/z [M+H]+ calc'd for C11H14BrN3, 268. found 268.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09371321B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-86bf7020f3bd40e9b45cd148bf117f47
출처 메모uspto-grants-2016_06