Piperidine → HCID 70926646, compound

HRID 1428469Notes

Reaction equation

HRID 1428469 reaction equation
[CH3:1][CH:2]=[CH:3][C:4]([C:6]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:7]=1[CH:8]=[CH:9][CH:10]=[CH:11]2)=[O:5].[NH:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[N:16]1([CH2:9][CH2:8][C:7]2[C:12]3[C:13](=[C:9]([CH3:10])[CH:8]=[CH:10][CH:11]=3)[CH:14]=[CH:15][C:6]=2[C:4]([C:3]2[CH:2]=[CH:1][C:7]3[C:6](=[CH:15][CH:14]=[CH:13][C:12]=3[CH3:11])[C:4]=2[CH2:3][CH2:2][N:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)=[O:5])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 85607810HCID 85607810, compound

Product 1

HCID 70926646HCID 70926646, compound

Procedure

5-methylacryloylnaphthalene (21.8 mg) and piperidine (9.1 mg) were reacted at 50° C. for 5 hours.

Sources & evidence

ORD record
ord-7dda2d070d1747d1b24f1ae5ee5c313a
Source dataset
uspto-grants-2015_01
Patent number
US08937091B2

Reaction notes

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