4-Thiazoleacetic acid, 2-amino-, ethyl ester → [2-(3,5-Diisopropoxy-benzoylamino)-thiazol-4-yl]acetic acid ethyl ester

HRID 1510303Notes

Reaction equation

HRID 1510303 reaction equation
[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([O:14][CH:15]([CH3:17])[CH3:16])[CH:13]=1)[C:8]([OH:10])=O)([CH3:3])[CH3:2].[NH2:18][C:19]1[S:20][CH:21]=[C:22]([CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[N:23]=1>>[CH2:28]([O:27][C:25](=[O:26])[CH2:24][C:22]1[N:23]=[C:19]([NH:18][C:8](=[O:10])[C:7]2[CH:11]=[C:12]([O:14][CH:15]([CH3:17])[CH3:16])[CH:13]=[C:5]([O:4][CH:1]([CH3:2])[CH3:3])[CH:6]=2)[S:20][CH:21]=1)[CH3:29]

Participants

3

Reactant 2

HCID 1044544-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 205341403,5-Diisopropoxybenzoic acid-1G

Product 1

HCID 24757170[2-(3,5-Diisopropoxy-benzoylamino)-thiazol-4-yl]acetic acid ethyl ester

Procedure

[2-(3,5-Diisopropoxy-benzoylamino)-thiazol-4-yl]acetic acid ethyl ester was prepared from 3,5-diisopropoxybenzoic acid (prepared as described in general synthetic descriptions B, using 2-bromopropane as alkylhalid) and ethyl 2-aminothiazol-4-ylacetate following synthetic description A.

Sources & evidence

ORD record
ord-cede2ca3432b484e965fac9036042669
Source dataset
uspto-grants-2012_07
Patent number
US08211925B2

Reaction notes

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