4-Benzylpiperidine → HCID 178521790, compound

HRID 2115017Notes

Reaction equation

HRID 2115017 reaction equation
[SH:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([NH:11][C:12](=[O:16])[C:13]([OH:15])=O)[CH:8]=[CH:7][C:5]=2[N:6]=1.[CH2:17]([CH:24]1[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C(OCC)C>[CH2:17]([CH:24]1[CH2:29][CH2:28][N:27]([C:13](=[O:15])[C:12]([NH:11][C:9]2[CH:8]=[CH:7][C:5]3[N:6]=[C:2]([SH:1])[NH:3][C:4]=3[CH:10]=2)=[O:16])[CH2:26][CH2:25]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

Participants

4

Reactant 2

HCID 317384-BenzylpiperidineHCID 178526016Oxo[(2-sulfanylidene-2,3-dihydro-1H-benzimidazol-5-yl)amino]acetic acid

Product 1

HCID 178521790HCID 178521790, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

The title compound is prepared from N-(2-mercapto-3H-benzimidazol-5-yl)-oxalamic acid and 4-benzyl-piperidine according to the method described in Example 1c. Melting Point: 277-281° C. (diethylether)

Sources & evidence

ORD record
ord-2ddf9d57b3d44189a4d46742fa3df79d
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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