Tyrosine Methyl Ester → HCID 69610138, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:14])[C@@H:4]([NH2:13])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1.[CH:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[C:17]([C:25](O)=[O:26])[N:16]=1>>[CH3:1][O:2][C:3](=[O:14])[C@@H:4]([NH:13][C:25]([C:17]1[N:16]=[CH:15][C:24]2[C:19]([CH:18]=1)=[CH:20][CH:21]=[CH:22][CH:23]=2)=[O:26])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1Participants
3
Procedure
3-(4-Hydroxyphenyl)-(2S)-[(isoquinoline-3-carbonyl)-amino]-propionic acid methyl ester (807 mg, 90%) was prepared from (2S)-amino-3-(4-hydroxy-phenyl)-propionic acid methyl ester (500 mg, 3.0 mmol) and isoquinoline-3-carboxylic acid (530 mg, 2.3 mmol) according to general procedure A.
Sources & evidence
- ORD record
- ord-751606ba90a3422fa0c96660c9a4c63a
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07122580B2
Reaction notes
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