Piperidine → HCID 70927016, compound

HRID 1428470Notes

Reaction equation

HRID 1428470 reaction equation
[CH:1]([C:3]1[C:12]2[C:7](=[C:8]([Cl:13])[CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][C:4]=1[C:14]([C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][C:22]=2[Cl:26])[C:17]=1[CH:27]=[CH2:28])=[O:15])=[CH2:2].[NH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1>ClCCl>[N:29]1([CH2:28][CH2:27][C:17]2[C:18]3[C:23](=[C:22]([Cl:26])[CH:21]=[CH:20][CH:19]=3)[CH:24]=[CH:25][C:16]=2[C:14]([C:4]2[CH:5]=[CH:6][C:7]3[C:12](=[CH:11][CH:10]=[CH:9][C:8]=3[Cl:13])[C:3]=2[CH2:1][CH2:2][N:29]2[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]2)=[O:15])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1

Participants

4

Reactant 2

HCID 8082PiperidineHCID 86673233HCID 86673233, compound

Product 1

HCID 70927016HCID 70927016, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Vinyl-5-chloro-2-naphthylketone (21.4 mg) and piperidine (8.4 mg) were reacted in dichloromethane (0.3 mL).

Sources & evidence

ORD record
ord-d766118764314cdcb3dfe22611b1d01f
Source dataset
uspto-grants-2015_01
Patent number
US08937091B2

Reaction notes

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