5-(2-acetyloxyethylcarbamoyl)-1H-indole-2-carboxylic acid → 6-{[5-(2-Acetoxyethylcarbamoyl)-1H-indole-2-carbonyl]amino}-1H-indole-2-carboxylic acid methyl ester

HRID 724535Notes

Reaction equation

HRID 724535 reaction equation
[CH3:1][O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[C:9]([NH:14]C(C1NC3C(C=1)=CC(C(=O)NCCNC(OC(C)(C)C)=O)=CC=3)=O)[CH:8]=2)=[O:4].[C:39]([O:42][CH2:43][CH2:44][NH:45][C:46]([C:48]1[CH:49]=[C:50]2[C:54](=[CH:55][CH:56]=1)[NH:53][C:52]([C:57]([OH:59])=O)=[CH:51]2)=[O:47])(=[O:41])[CH3:40]>>[CH3:1][O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[C:9]([NH:14][C:57]([C:52]1[NH:53][C:54]3[C:50]([CH:51]=1)=[CH:49][C:48]([C:46](=[O:47])[NH:45][CH2:44][CH2:43][O:42][C:39](=[O:41])[CH3:40])=[CH:56][CH:55]=3)=[O:59])[CH:8]=2)=[O:4]

Participants

3

Procedure

Compound 151 is synthesized as described for compound 39 in Example 33 except instead of compound 3, compound 150 is used.

Sources & evidence

ORD record
ord-3fee7d91870e4d05b74b7246c10be883
Source dataset
uspto-grants-2006_11
Patent number
US07141680B2

Reaction notes

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