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HRID 1480170作成日:2026年10月25日

Benzyl chloroformate → (1-Cyano-2-methanesulfonyl-1-methyl-ethyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/1480170

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl chloroformateHCID 10387—
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-3-methanesulfonyl-2-methyl-propionitrileHCID 90203372—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Cyano-2-methanesulfonyl-1-methyl-ethyl)-carbamic acid benzyl esterHCID 9020404889%

反応条件

温度45 °C

反応手順

To a solution of 2-Amino-3-methanesulfonyl-2-methyl-propionitrile (Example 80a, 5.01 g, 30.9 mmol) in dry THF (119 mL) was added DIEA (12.1 mL, 67.9 mmol) and benzyl carbonochloridate (CAN 501-53-1, 5.57 mL, 37.1 mmol). Reaction was stirred at 45° C. for 18 hours. The reaction mixture was concentrated in vacuo. The residue was dissolved in ethylacetate and was extracted with an 1.0M aqueous solution of sodium bicarbonate. The organic layer was dried over sodium sulfate and evaporated down to dryness. The crude was purified by flash chromatography on silica eluting with a heptane/ethyl acetate gradient to yield the title compound (8.12, 89%) as a yellow oil. MS (ESI, m/z): 297.5 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09409866B2
出典データセットuspto-grants-2016_08
ORD IDord-ac3eb25091604f1da2dc47aee08679fb
出典メモuspto-grants-2016_08