Amidinothiourea → HCID 178468676, compound

HRID 12043

Reaction equation

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

Participants

Reactant 2

HCID 2724563Amidinothiourea

HCID 12917737Ethyl 3-bromo-4-oxocyclohexane-1-carboxylate

Product 1

HCID 178468676HCID 178468676, compound

Procedure

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

Sources & evidence

ORD record: ord-36e7a4e2ac1d496fa174c9edc625682a
Source dataset: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07727979B2

Linked notes

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