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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1013602생성일: 2026년 10월 25일

Triethylamine → acetic acid {[(R)-6-(3-fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl ester

https://huagongshe.com/reaction/1013602

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물AcetoxyacetoneHCID 11593—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물C-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-yl]-methylamine hydrochlorideHCID 66651558—
용매DichloromethaneHCID 6344—
생성물acetic acid {[(R)-6-(3-fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl esterHCID 5920718270.5%

반응 단계

C-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-yl]-methylamine hydrochloride (0.12 gms, 0.338 mmole), 1-hydroxybenzotriazol (0.07 g, 0.507 mmol) ethylcarbodiimide (0.10 g, 0.507 mmol), triethylamine (0.3 mL, 2.0 mmol) and acetic acid 2-oxo-propyl ester (0.05 g, 0.40 mmol) were dissolved in 10 mL methylene chloride. The reaction mixture was stirred at room temperature for 24 hours. The reaction was quenched with water, and the entire mixture was absorbed on to silica gel and medium pressure chromatography, and eluted with ethyl acetate/hexanes (3:1) to give 0.1 g of acetic acid {[(R)-6-(3-fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981923B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-53a5d1106e984c99b3437b32f9f5895b
출처 메모uspto-grants-2011_07