HCID 9931836, compound → HCID 86755683, compound

HRID 1872227Notes

Reaction equation

C(OC([C@H]1[C@H](CC2C=CC=CC=2)CCCC(=O)N1)=O)C.[OH:21][NH:22][C:23]([C@H:25]1[C@@H:31]([CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH2:30][CH2:29][CH2:28][CH2:27][N:26]1[S:39]([C:42]1[CH:47]=[CH:46][C:45]([O:48][CH3:49])=[CH:44][CH:43]=1)(=[O:41])=[O:40])=[O:24]>>[OH:21][NH:22][C:23]([C@H:25]1[C@H:31]([CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH2:30][CH2:29][CH2:28][CH2:27][N:26]1[S:39]([C:42]1[CH:47]=[CH:46][C:45]([O:48][CH3:49])=[CH:44][CH:43]=1)(=[O:41])=[O:40])=[O:24]

Participants

Reactant 2

HCID 9931836HCID 9931836, compound

HCID 70074993HCID 70074993, compound

Product 1

HCID 86755683HCID 86755683, compound

Procedure

trans-3-Benzyl-1-(4-methoxybenzenesulfonyl)-azepane-2-carboxylic acid-hydroxyamide was synthesized from trans-3-Benzyl-7-oxo-azepane-2-carboxylic acid ethyl ester using the procedures for the preparation of cis-3-Benzyl-1-(4-methoxybenzenesulfonyl)-azepane-2-carboxylic acid-hydroxyamide.

Sources & evidence

ORD record: ord-cd6833e1b8224736a9917a07c0ea4acf
Source dataset: uspto-grants-2000_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06107291

Reaction notes

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