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HRID 250305作成日:2026年10月25日

Diisopropylethylamine → (R)-3-tert-Butoxy-2-[(1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-amino]-propionic acid tert-butyl ester

https://huagongshe.com/reaction/250305

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-Chloro-4-hydroxyisoquinoline-3-carboxylic acidHCID 11020520—
反応物H-D-Ser(tBu)-OtBu.HClHCID 56777372—
反応物HCID 178484681HCID 178484681—
溶媒DichloromethaneHCID 6344—
生成物(R)-3-tert-Butoxy-2-[(1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-amino]-propionic acid tert-butyl esterHCID 8659544731.9%

反応手順

To a mixture of 45 mg (0.2 mmol) of 1-chloro-4-hydroxy-isoquinoline-3-carboxylic acid, 76 mg (0.2 mmol) of benzotriazol-1-yl-(bis-dimethylamino-methylene)-oxonium hexafluoro phosphate (HBTU), 50.8 mg (R)-2-amino-3-tert-butoxy-propionic acid tert-butyl ester hydrochloride (0.2 mmol), and 1 ml of dichloromethane was added 122.5 μl (0.7 mmol) of ethyl-diisopropyl-amine with stirring. Stirring was continued at ambient temperature for 40 h. The product was isolated from the reaction mixture by flash column chromatography on silica gel using hexanes:ethyl acetate (9:1) as the eluent to give a colorless oil. 27 mg of the title compound was obtained; MS-(+)-ion: M+1=422.8 amu.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863292B2
出典データセットuspto-grants-2011_01
ORD IDord-114dfef9e9f945789a3704cb787d3fe2
出典メモuspto-grants-2011_01