4-[(4-Fluorophenyl)(phenyl)methylidene]piperidine → HCID 67895758, compound

HRID 1460451Notes

Reaction equation

HRID 1460451 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][CH2:24][N:25]1[C:30](=[O:31])[CH2:29][N:28]([CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][N:34]=2)[CH2:27][C:26]1=[O:39]>>[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][CH2:24][N:25]3[C:30](=[O:31])[CH2:29][N:28]([CH2:32][C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][N:34]=4)[CH2:27][C:26]3=[O:39])[CH2:13][CH2:14]2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 150203584-[(4-Fluorophenyl)(phenyl)methylidene]piperidineHCID 199157521-(3-Chloropropyl)-4-(2-pyridylmethyl)-2,6-piperazinedione

Product 1

HCID 67895758HCID 67895758, compound

Procedure

This compound was prepared from 4-[(4-fluorophenyl)phenylmethylene]piperidine and 1-(3-chloropropyl)-4-(2-pyridylmethyl)-2,6-piperazinedione according to the process described in Example 6, Stage E.

Sources & evidence

ORD record
ord-05aed93225cd4549b12080a1ec59e8ec
Source dataset
uspto-grants-1991_12
Patent number
US05071847

Reaction notes

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