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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43008생성일: 2026년 10월 23일

Triethylamine → (R)-N-(5((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-2-yl)-2-chlorobenzenesulfonamide

https://huagongshe.com/ko/reaction/43008

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Chlorobenzenesulfonyl chlorideHCID 76187—
반응물(R)-(1-((2-amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanolHCID 67026260—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물(R)-N-(5((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-2-yl)-2-chlorobenzenesulfonamideHCID 6708813931.5%

반응 단계

(R)-(1-((2-amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol (0.064 mmol, 20 mg) was dissolved in tetrahydrofuran (1 mL) and triethylamine (0.128 mmol, 17.8 μL) followed by 2-chlorobenzenesulfonyl chloride (0.064 mmol, 13.6 mg) and the solution stirred at room temperature overnight. The reaction was concentrated to dryness to give a brown residue which was dissolved in DMSO (1 mL) and purified on preparative basic HPLC to give the title compound (9.8 mg, 0.02 mmol, 31.5%) MS (ESI): m/z [M−H]− 484.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536214B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5a0c0cfd30e44d2c80d473cec7dc8547
출처 메모uspto-grants-2013_09