4-Benzylpiperidine → HCID 9947261, compound

HRID 2115078Notes

Reaction equation

HRID 2115078 reaction equation
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:15]=[CH:14][C:9]2[NH:10][C:11](=[O:13])[O:12][C:8]=2[CH:7]=1)=[O:4].[CH2:16]([CH:23]1[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>O>[CH2:16]([CH:23]1[CH2:28][CH2:27][N:26]([CH2:2][C:3]([NH:5][C:6]2[CH:15]=[CH:14][C:9]3[NH:10][C:11](=[O:13])[O:12][C:8]=3[CH:7]=2)=[O:4])[CH2:25][CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

4

Reactant 2

HCID 317384-BenzylpiperidineHCID 1132892HCID 1132892, compound

Product 1

HCID 9947261HCID 9947261, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The title compound is prepared from 2-chloro-N-(2-oxo-2,3-dihydro-benzoxazol-6-yl)-acetamide (Example 142a) and 4-benzyl-piperidine according to the method described in Example 142b. Melting Point: 210-212° C. (water)

Sources & evidence

ORD record
ord-ff07fa90144d45669754f02606cd7ba5
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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