Pivaloyl-L-phenylalanine → HCID 178501412, compound

HRID 1590124Notes

Reaction equation

HRID 1590124 reaction equation
[C:1]([NH:7][C@H:8]([C:16]([OH:18])=O)[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].[CH3:19][O:20][C:21](=[O:42])[C@H:22]([CH2:36][C:37]1[N:41]=[CH:40][NH:39][CH:38]=1)[NH:23][C:24](=[O:35])[C@H:25]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[NH:26][CH3:27]>>[CH3:19][O:20][C:21](=[O:42])[C@H:22]([CH2:36][C:37]1[N:41]=[CH:40][NH:39][CH:38]=1)[NH:23][C:24](=[O:35])[C@H:25]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[N:26]([C:16](=[O:18])[C@H:8]([CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[NH:7][C:1](=[O:6])[C:2]([CH3:3])([CH3:4])[CH3:5])[CH3:27]

Participants

3

Procedure

N-Pivaloyl-L-phenylalanine and N-methyl-L-phenylalanyl-L-histidine methyl ester are treated in the same manner as described in Example 1 to give N-pivaloyl-L-phenylalanyl-N-methyl-L-phenylalanyl-L-histidine methyl ester.

Sources & evidence

ORD record
ord-c3b7121b3f664533b44ce39b6daf7e2a
Source dataset
uspto-grants-1993_04
Patent number
US05202312

Reaction notes

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