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HRID 63716作成日:2026年10月26日

2,6-Dichlorobenzoyl chloride → (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester

https://huagongshe.com/reaction/63716

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dichlorobenzoyl chlorideHCID 78392—
反応物DiisopropylethylamineHCID 81531—
反応物4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
溶媒DichloromethaneHCID 6344—
生成物(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl esterHCID 5439386188.5%

反応手順

To a solution of (S)-3-[4-aminophenyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester (37.57 g, 127.6 mmol) and 2,6-dichlorobenzoyl chloride (29.45 g, 140.6 mmol) in dichloromethane (350 mL) was added DIPEA (24.8 g, 192 mmol) at room temperature. The brown solution was stirred for 15 h at room temperature to afford a white suspension at this time TLC analysis of the mixture indicated the absence of starting material. Then, the solids were collected by filtration and the solids were washed with dichloromethane (150 mL) and air dried to obtain 52.75 g (88.4% yield) of (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester as a white solid: mp 192-194° C. ES(+)-HRMS m/e calcd. for C22H24Cl2N2O5 (M+H)+ 466.1062, obsd. 466.1069.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447035B2
出典データセットuspto-grants-2016_09
ORD IDord-ec259c0dcfa745ae80aa81e4c827b872
出典メモuspto-grants-2016_09