Ethyl 3-bromo-2-oxocyclohexanecarboxylate → HCID 178468780, compound

HRID 12040

Reaction equation

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

Participants

Reactant 2

HCID 121765Ethyl 3-bromo-2-oxocyclohexanecarboxylate

HCID 2724563Amidinothiourea

Product 1

HCID 178468780HCID 178468780, compound

Procedure

Analogously to the preparation of Example C-01, 3-bromo-2-oxo-cyclohexane carboxylic acid ethyl ester is reacted with 2-imino-4-thiobiuret to produce the title compound.

Sources & evidence

ORD record: ord-b69ffd70b70b453990f6ee758973e6dd
Source dataset: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07727979B2

Linked notes

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