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HRID 51864作成日:2026年10月27日

2,2,2-Trichloroethyl chloroformate → (2-Benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester

https://huagongshe.com/reaction/51864

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,2-Trichloroethyl chloroformateHCID 87063—
反応物N-{7-[bis-(4-methyl-benzyl)-amino]-4-methoxy-benzothiazol-2-yl}-benzamideHCID 22015745—
溶媒AcetonitrileHCID 6342—
生成物(2-Benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl esterHCID 8658901940.4%

反応条件

温度80 °C

反応手順

To a stirred solution of 300 mg (0.59 mmol) N-{7-[bis-(4-methyl-benzyl)-amino]-4-methoxy-benzothiazol-2-yl}-benzamide in 10 ml acetonitrile was added dropwise 0.60 ml (4.46 mmol) 2,2,2-trichloroethyl chloroformate and the reaction mixture heated at 80° C. for 72 h. The mixture was then concentrated in vacuo. Flash chromatography (ethyl acetate/hexane) afforded 138 mg (40%) (2-benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester as a yellow solid. ES-MS m/e (%):584 (M{37Cl, 37Cl, 37Cl}+H+, 5), 582 (M{37Cl, 37Cl, 35Cl}+H+, 32), 580 (M{37Cl, 35Cl, 35Cl}+H+, 100), 578 (M{35Cl, 35Cl, 35Cl}+H+, 92).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713499B2
出典データセットuspto-grants-2004_03
ORD IDord-72ea1724071f4980b0661692dda3e538
出典メモuspto-grants-2004_03