Piperidine → HCID 68579817, compound

HRID 446867Notes

Reaction equation

HRID 446867 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:25][C:26]2[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=2)=[C:6]([NH:8][S:9]([C:12]2[CH:24]=[CH:23][C:15]([C:16]([NH:18][CH2:19][C:20]([OH:22])=O)=[O:17])=[CH:14][CH:13]=2)(=[O:11])=[O:10])[CH:7]=1.[NH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:25][C:26]2[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=2)=[C:6]([NH:8][S:9]([C:12]2[CH:24]=[CH:23][C:15]([C:16]([NH:18][CH2:19][C:20](=[O:22])[N:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)=[O:17])=[CH:14][CH:13]=2)(=[O:11])=[O:10])[CH:7]=1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 68577396HCID 68577396, compound

Product 1

HCID 68579817HCID 68579817, compound

Procedure

The title compound was prepared from {4-[5-fluoro-2-(4-fluoro-phenoxy)-phenylsulfamoyl]-benzoylamino}-acetic acid and piperidine according to the method described in Example 1.1/f. MS (EI) 533.3 (MH+).

Sources & evidence

ORD record
ord-de5289c3c6f34c8ea76f87d0602dd66a
Source dataset
uspto-grants-2013_07
Patent number
US08481527B2

Reaction notes

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