4-[(4-Fluorophenyl)(phenyl)methylidene]piperidine → HCID 67896095, compound

HRID 1089764Notes

Reaction equation

HRID 1089764 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[CH:4][CH:3]=1.[Cl:21][CH2:22][CH2:23][N:24]1[C:29](=[O:30])[CH2:28][N:27]([CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=2)[CH2:26][C:25]1=[O:38]>>[ClH:21].[ClH:21].[ClH:21].[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[C:9]2[CH2:10][CH2:11][N:12]([CH2:22][CH2:23][N:24]3[C:25](=[O:38])[CH2:26][N:27]([CH2:31][C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=4)[CH2:28][C:29]3=[O:30])[CH2:13][CH2:14]2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 150203584-[(4-Fluorophenyl)(phenyl)methylidene]piperidineHCID 19915777HCID 19915777, compound

Product 1

HCID 67896095HCID 67896095, compound

Procedure

This compound was prepared from 4-[(4-fluorophenyl)phenylmethylene]piperidine and 1-(2-chloroethyl)-4-(2-pyridylmethyl)-2,6-piperazinedione according to the process described in Example 6, Stage E.

Sources & evidence

ORD record
ord-5c078145931447b5ba56c6756dd30d10
Source dataset
uspto-grants-1992_01
Patent number
US05079249

Reaction notes

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