3-Amino-5,5-dimethyl-2-cyclohexen-1-one → HCID 22117811, compound

HRID 1740424Notes

Reaction equation

HRID 1740424 reaction equation
[NH2:1][C:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4](=[O:10])[CH:3]=1.[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][C:13]=1[F:20]>>[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]2[C:3]3[C:4](=[O:10])[CH2:5][C:6]([CH3:9])([CH3:8])[CH2:7][C:2]=3[NH:1][C:2]3[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4](=[O:10])[C:3]2=3)=[CH:14][C:13]=1[F:20]

Participants

3

Reactant 2

HCID 1366803-Amino-5,5-dimethyl-2-cyclohexen-1-oneHCID 27249854-Chloro-3-Fluorobenzaldehyde

Product 1

HCID 22117811HCID 22117811, compound

Procedure

Reaction of 3-amino-5,5-dimethyl-2-cyclohexen-1-one with 4-chloro-3-fluorobenzaldehyde in an analogous manner to that described in Example 1 gave 9-(4-chloro-3-fluorophenyl)-3,4,6,7,9,10-hexahydro-3,3,6,6-tetramethyl-1,8(2H,5H)-acridinedione. Crystallization from absolute ethanol gave a yellow crystalline solid of melting point >300° C. (decomposition).

Sources & evidence

ORD record
ord-d1e476b7009045518c8187bc95af4334
Source dataset
uspto-grants-1999_10
Patent number
US05969139

Reaction notes

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