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HRID 216923作成日:2026年10月25日

Methyl N-(triethylammoniosulfonyl)carbamate → (S)-tert-butyl 4-(1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216923

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
反応物(S)-tert-Butyl 4-(1-amino-3-(3'-cyanobiphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568564—
溶媒DichloromethaneHCID 6344—
生成物(S)-tert-butyl 4-(1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 5956858892.6%

反応手順

(S)-tert-Butyl 4-(1-amino-3-(3′-cyanobiphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 8, step (i), 316 mg) in dichloromethane (8 mL) was treated with Burgess' reagent (306 mg) and the mixture was stirred at room temperature for 18 h. The solvent was partially evaporated and the solution was purified by chromatography on silica using ethyl acetate/isohexane and then ethyl acetate as eluent to afford the sub-titled compound as a white solid (282 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193239B2
出典データセットuspto-grants-2012_06
ORD IDord-bf4e9b47d2c7465fbbc95e5b1390c0c8
出典メモuspto-grants-2012_06