Hydrochloric Acid → Hydrochloric Acid
Reaction equation
[NH:1](C(OC(C)(C)C)=O)[C@@H:2]([C:9]([OH:11])=O)[CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.[NH:19]1[CH2:26][CH2:25][CH2:24][C@H:20]1[C:21]([OH:23])=[O:22].[C:27]([C:29]1[CH:36]=[CH:35][C:32]([CH2:33][NH-:34])=[CH:31][CH:30]=1)#[N:28].[ClH:37]>>[NH2:1][C@@H:2]([C:9]([N:19]1[CH2:26][CH2:25][CH2:24][C@H:20]1[C:21]([OH:23])=[O:22])=[O:11])[CH:3]1[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1.[C:27]([C:29]1[CH:36]=[CH:35][C:32]([CH2:33][NH-:34])=[CH:31][CH:30]=1)#[N:28].[ClH:37]Participants
5
Procedure
Firstly H-(D)-Chg-Pro-p-cyanobenzylamide×HCl was prepared from Boc-(D)-Chg-OH and H-Pro-p-cyanobenzylamide×HCl as in Example 3.
Sources & evidence
- ORD record
- ord-24fa8cfdeec54d99bd89d7e5cb81caca
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06455671B1
Reaction notes
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