Hydrochloric Acid → (S)-2-[(6-Isopropoxy-1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-amino]-propionic acid
反応式
[CH:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11]([Cl:15])=[N:10][C:9]([C:16]([OH:18])=O)=[C:8]2[OH:19])([CH3:3])[CH3:2].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C[O:45][C:46](=[O:50])[C@H:47]([CH3:49])[NH2:48].[OH-].[Na+].Cl>CO.O>[CH:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11]([Cl:15])=[N:10][C:9]([C:16]([NH:48][C@@H:47]([CH3:49])[C:46]([OH:50])=[O:45])=[O:18])=[C:8]2[OH:19])([CH3:2])[CH3:3]参加物
7
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
0.030 g of 6-isopropoxy-1-chloro-4-hydroxy-isoquinoline-3-carboxylic acid and 0.046 g of HATU were allowed to react with 0.017 g of L-Alanine methyl ester under analogous conditions to Example A-1 a). Treatment of the crude product ester with 0.014 g of NaOH in 0.1 ml of 1:1 methanol-water at room temperature for 2 days, followed by acidification to pH=2 with 1M hydrochloric acid, gave a solid product. The product was collected by filtration, washed with water, and dried to give 0.023 g of an off-white solid: MS-(−)-ion, M−1=353.0 amu.
後処理
- customgave a solid product
- filtrationThe product was collected by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-0ed315bc12c14421a015d790a1dea234
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07863292B2
反応ノート
読み込み中…