HCID 9931836, compound → HCID 86755684, compound

HRID 1872228Notes

Reaction equation

HRID 1872228 reaction equation
C(OC(C1(C2C=CC=CC=2)CCCC(=O)CN1)=O)C.[OH:20][NH:21][C:22]([C@H:24]1[C@@H:30]([CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34]C=2)[CH2:29][CH2:28][CH2:27][CH2:26][N:25]1[S:38]([C:41]1[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[CH:43][CH:42]=1)(=[O:40])=[O:39])=[O:23]>>[C:31]1([C@@H:30]2[CH2:29][CH2:28][CH2:27][CH2:26][N:25]([S:38]([C:41]3[CH:42]=[CH:43][C:44]([O:47][CH3:48])=[CH:45][CH:46]=3)(=[O:39])=[O:40])[C@H:24]2[C:22]([NH:21][OH:20])=[O:23])[CH:32]=[CH:37][CH:36]=[CH:35][CH:34]=1

Participants

3

Reactant 2

HCID 9931836HCID 9931836, compoundHCID 53905062HCID 53905062, compound

Product 1

HCID 86755684HCID 86755684, compound

Procedure

trans-3-Phenyl-1-(4-methoxybenzenesulfonyl)-azepane-2-hydroxamic acid was synthesized from 2-Phenyl-6-oxo-azepane 2-carboxylic acid ethyl ester in the same manner as the procedures used for the preparation of cis-3-Benzyl-1-(4-methoxybenzenesulfonyl)-azepane-2-carboxylic acid-hydroxyamide.

Sources & evidence

ORD record
ord-e2fc21f795f64255b12208f6a15f3979
Source dataset
uspto-grants-2000_08
Patent number
US06107291

Reaction notes

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