Ethyl 2-oxocyclohexylacetate → HCID 17913378, compound

HRID 1382831Notes

Reaction equation

HRID 1382831 reaction equation
Cl.[Cl:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][N:8]([C:10]2[CH:15]=[CH:14][C:13]([S:16][CH3:17])=[CH:12][CH:11]=2)N)=[CH:5][CH:4]=1.CC[O:22][C:23]([CH2:25][CH:26]1[C:31](=O)[CH2:30][CH2:29][CH2:28][CH2:27]1)=[O:24]>>[Cl:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][N:8]2[C:27]3[CH:26]([CH2:25][C:23]([OH:24])=[O:22])[CH2:31][CH2:30][CH2:29][C:28]=3[C:15]3[C:10]2=[CH:11][CH:12]=[C:13]([S:16][CH3:17])[CH:14]=3)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 91229Ethyl 2-oxocyclohexylacetateHCID 67867375HCID 67867375, compound

Product 1

HCID 17913378HCID 17913378, compound

Procedure

Following the procedure of Example 1, but using 1-(4-chlorobenzyl)-1-(4-methylthiophenyl)hydrazine hydrochloride and ethyl 2-cyclohexanone acetate as starting materials, the title compound was prepared.

Sources & evidence

ORD record
ord-2da296c0ed974e1c95d1fde69e058f9d
Source dataset
uspto-grants-1989_02
Patent number
US04808608

Reaction notes

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