Isopropylamine → HCID 131729398, compound

HRID 421175Notes

Reaction equation

[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:30])=[C:6]([CH:29]=1)[C:7]([NH:9][C:10]1[S:11][C:12]([C:26](O)=[O:27])=[C:13]([C:15]2[C:20]([F:21])=[C:19]([F:22])[C:18]([F:23])=[C:17]([F:24])[C:16]=2[F:25])[N:14]=1)=[O:8].[CH:31]([NH2:34])([CH3:33])[CH3:32]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:30])=[C:6]([CH:29]=1)[C:7]([NH:9][C:10]1[S:11][C:12]([C:26]([NH:34][CH:31]([CH3:33])[CH3:32])=[O:27])=[C:13]([C:15]2[C:20]([F:21])=[C:19]([F:22])[C:18]([F:23])=[C:17]([F:24])[C:16]=2[F:25])[N:14]=1)=[O:8]

Participants

Reactant 2

HCID 6363Isopropylamine

HCID 17860265HCID 17860265, compound

Product 1

HCID 131729398HCID 131729398, compoundYield 23.9%

Procedure

Using 2-(5-bromo-2-hydroxybenzoyl)amino-4-(pentafluorophenyl)-thiazole-5-carboxylic acid and isopropylamine as the raw materials, the same operation as the example 212(2) gave the title compound.

Sources & evidence

ORD record: ord-67bf5283099041c19d7aec12fb3b7e26
Source dataset: uspto-grants-2012_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08097759B2

Reaction notes

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