HCID 13393252、化合物 → HCID 13606280、化合物
反応式
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]([CH2:11][CH:12]([NH2:16])[C:13]([OH:15])=[O:14])[C:3]1=[O:17].[Cl:18][C:19]1[CH:36]=[CH:35][C:22]([C:23](N2C3C=CC=CC=3OC2=S)=[O:24])=[CH:21][CH:20]=1>CN1CCCC1=O>[Cl:18][C:19]1[CH:36]=[CH:35][C:22]([C:23]([NH:16][CH:12]([CH2:11][CH:4]2[C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[N:2]([CH3:1])[C:3]2=[O:17])[C:13]([OH:15])=[O:14])=[O:24])=[CH:21][CH:20]=1参加物
4
実験手順
2 Grams of 3-(1-methyloxindol-3-yl)-2-aminopropionic acid prepared in Reference Example 5 was suspended in 50 ml of 1-methyl-2-pyrrolidone, then 2.2 g of 3-(4-chlorobenzoyl)benzoxazolin-2-thione was added thereto, and the reaction mixture was stirred at a room temperature for 3 days. The reaction mixture was poured into an ice-water, and the crystals formed were collected by filtration, then the crystals were dissolved in 1N-sodium hydroxide aqueous solution, then the resulting solution was acidified by using 10%-hydrochloric acid, and the crystals formed were collected by filtration. The crystals were dried, washed with chloroform, there was obtained 1.1 g of 2-(4-chlorobenzoylamino)-3-(1-methyloxindol-3-yl)propionic acid. White powdery substance. Melting point: 115°-120° C.