戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 526323作成日:2026年10月25日

Cesium carbonate → tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioate

https://huagongshe.com/reaction/526323

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl methyl malonateHCID 2733872—
反応物1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1R,2R)-(-)-2-(dimethylamino)cyclohexyl]thiourea(R,R-TUC)HCID 11486766—
反応物Tert-butyl {[3-(benzyloxy)phenyl](phenylsulfonyl)methyl}carbamateHCID 71268083—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioateHCID 117653877—

反応条件

温度0 °C

反応手順

Tert-butyl {[3-(benzyloxy)phenyl](phenylsulfonyl)methyl}carbamate (3.0 g, 5.93 mmol) was suspended in a toluene (21.6 mL) water (16 mL) mixture. At 0° C. tert-butyl methyl malonate (1.2 mL, 7.1 mmol), cesium carbonate (1.94 g, 5.9 mmol) and 1-[3,5-bis(trifluoromethy) phenyl]-3-[(1R,2R)-(−)-2-(dimethylamino)cyclohexyl]thiourea (246 mg, 0.59 mmol) was added and the mixture was stirred for 72 hours at 0° C. After storage at −20° C. for 72 hours the mixture was diluted with water and ethyl acetate, after filtration the phases were separated and the aqueous phase extracted with ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (ethyl acetate in hexane 0 to 35%) to yield 2.17 g of enantiomerically enriched tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09345793B2
出典データセットuspto-grants-2016_05
ORD IDord-91abd16de4f848ec89b86b9eb7815cf1
出典メモuspto-grants-2016_05