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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | Thiomorpholine 1-oxide | HCID 12600299 | — |
| 반응물 | 6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehyde | HCID 59331419 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 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 | HCID 59331300 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08318746B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-4045f70aa5de40ee8108d945ea3e753b |
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| 출처 메모 | uspto-grants-2012_11 |
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