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HRID 1013602作成日:2026年10月26日

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

https://huagongshe.com/reaction/1013602

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物AcetoxyacetoneHCID 11593—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物C-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-yl]-methylamine hydrochlorideHCID 66651558—
溶媒DichloromethaneHCID 6344—
生成物acetic acid {[(R)-6-(3-fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl esterHCID 5920718270.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981923B2
出典データセットuspto-grants-2011_07
ORD IDord-53a5d1106e984c99b3437b32f9f5895b
出典メモuspto-grants-2011_07