Aniline → HCID 69346672, compound
Reaction equation
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:22]([OH:24])=O)[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[NH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[C:26]1([NH:25][C:22](=[O:24])[C@H:9]([CH2:10][C:11]2[CH:12]=[CH:13][C:14]([O:17][C:18]([CH3:20])([CH3:21])[CH3:19])=[CH:15][CH:16]=2)[NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1Participants
3
Procedure
Using N-(tert-butoxycarbonyl)-(O-tert-butyl)-L-tyrosine and aniline, and in the same manner as in the method described in Example 1 (3), synthesis was performed.
Sources & evidence
- ORD record
- ord-e8e38d44df274aed99cd7ef0ef1d5f35
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06989401B2
Reaction notes
Loading…