4-Phenoxypiperidine → HCID 69100204, compound

HRID 2115153Notes

Reaction equation

HRID 2115153 reaction equation
Cl.[CH3:2][S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][CH2:14][C:15]([OH:17])=O)=[CH:9][CH:8]=1)(=[O:5])=[O:4].[O:18]([CH:25]1[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(OCC)C>[O:17]=[C:15]([N:28]1[CH2:29][CH2:30][CH:25]([O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:26][CH2:27]1)[CH2:14][NH:13][C:10]1[CH:9]=[CH:8][C:7]([NH:6][S:3]([CH3:2])(=[O:4])=[O:5])=[CH:12][CH:11]=1

Participants

4

Reactant 2

HCID 188784-PhenoxypiperidineHCID 69100191HCID 69100191, compound

Product 1

HCID 69100204HCID 69100204, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

The title compound is prepared from (4-methanesulfonylamino-phenylamino)-acetic acid hydrochloride and 4-phenoxy-piperidine according to the method described in Example 1c. Melting Point: 179-182° C. (diethylether)

Sources & evidence

ORD record
ord-84b21814e6454a5c81e9ffd067691200
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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