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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1881980생성일: 2026년 10월 26일

Sodium triacetoxyborohydride → 4-{[6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]methyl}thiomorpholine 1-oxide

https://huagongshe.com/reaction/1881980

반응식

참여 물질

역할이름HCID투입량
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Thiomorpholine 1-oxideHCID 12600299—
반응물6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehydeHCID 59331419—
용매1,2-DichloroethaneHCID 11—
용매Ethyl AcetateHCID 8857—
생성물4-{[6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]methyl}thiomorpholine 1-oxideHCID 5933130036%

반응 단계

To a solution of 6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehyde (200 mg) in 1,2-dichloroethane (5 mL) was added thiomorpholine 1-oxide (155 mg), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added sodium triacetoxyborohydride (280 mg), and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (87 mg, yield 36%) was obtained as a colorless amorphous solid from a fraction eluted with ethyl acetate. MS: 568 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08318746B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-4045f70aa5de40ee8108d945ea3e753b
출처 메모uspto-grants-2012_11