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HRID 253565作成日:2026年10月26日

4-(Aminomethyl)benzonitrile → tert-butyl (2S,3R)-4-(4-cyanobenzylamino)-1-cyclohexyl-3-hydroxybutan-2-ylcarbamate

https://huagongshe.com/reaction/253565

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Aminomethyl)benzonitrileHCID 82608—
反応物erythro-N-Boc-L-cyclohexylalanine epoxideHCID 9816868—
溶媒AcetonitrileHCID 6342—
生成物tert-butyl (2S,3R)-4-(4-cyanobenzylamino)-1-cyclohexyl-3-hydroxybutan-2-ylcarbamateHCID 5778647258%

反応手順

To a solution of tert-butyl (S)-2-cyclohexyl-1-((S)-oxiran-2-yl)ethylcarbamate (67.3 mg, 0.25 mmol) in CH3CN (8 mL) was added 4-cyanobenzylamine (39.6 mg, 0.3 mmol) and the mixture was heated under reflux overnight. The solvent was removed in vacuo and the residue was purified by the preparative HPLC to give tert-butyl (2S,3R)-4-(4-cyanobenzylamino)-1-cyclohexyl-3-hydroxybutan-2-ylcarbamate (58 mg, 58%). 1H NMR: 0.82 (m, 1H), 0.95 (m, 1H), 1.10-1.48 (m, 5H), 1.45 (s, 9H), 1.55-1.68 (m, 5H), 1.76 (m, 1H), 2.65 (m, 2H), 3.46 (m, 1H), 3.85 (m, 2H), 4.49 (m, 1H), 7.42 (d, 2H), 7.59 (d, 2H). MS (E/Z): 402 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872028B2
出典データセットuspto-grants-2011_01
ORD IDord-7aacd091071646e98274e8610343ad47
出典メモuspto-grants-2011_01