Isobutyryl chloride → N-[5-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-yl]-isobutyramide

HRID 604508Notes

Reaction equation

[CH2:1]([C:3]1[N:7]=[C:6]([C:8]2[S:12][C:11]([NH2:13])=[N:10][C:9]=2[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[O:5][N:4]=1)[CH3:2].[C:20](Cl)(=[O:24])[CH:21]([CH3:23])[CH3:22]>>[CH2:1]([C:3]1[N:7]=[C:6]([C:8]2[S:12][C:11]([NH:13][C:20](=[O:24])[CH:21]([CH3:23])[CH3:22])=[N:10][C:9]=2[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[O:5][N:4]=1)[CH3:2]

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 86630706HCID 86630706, compound

Product 1

HCID 11638722N-[5-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-yl]-isobutyramide

Procedure

Prepared from 5-(3-ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-ylamine and isobutyryl chloride.

Sources & evidence

ORD record: ord-572e8634bcf34752ad211879b62399b5
Source dataset: uspto-grants-2011_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07910613B2

Reaction notes

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