3-Hydroxypiperidine → Rac-2-(3-hydroxy-piperidin-1-yl)-5-methylsulfamoyl-benzoic acid

HRID 736216Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 736216
CS(C1C=CC(N2CCCC2)=C(C=1)C(O)=O)(=O)=O.Cl[C:20]1[CH:28]=[CH:27][C:26]([S:29](=[O:33])(=[O:32])[NH:30][CH3:31])=[CH:25][C:21]=1[C:22]([OH:24])=[O:23].[OH:34][CH:35]1[CH2:40][CH2:39][CH2:38][NH:37][CH2:36]1>>[OH:34][CH:35]1[CH2:40][CH2:39][CH2:38][N:37]([C:20]2[CH:28]=[CH:27][C:26]([S:29](=[O:33])(=[O:32])[NH:30][CH3:31])=[CH:25][C:21]=2[C:22]([OH:24])=[O:23])[CH2:36]1

Komponenten

4

Edukt 3

HCID 232933-HydroxypiperidineHCID 111724Benzoic acid, 2-chloro-5-[(methylamino)sulfonyl]-HCID 597934895-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid

Produkt 1

HCID 59793580Rac-2-(3-hydroxy-piperidin-1-yl)-5-methylsulfamoyl-benzoic acidAusbeute 15 %

Versuchsvorschrift

The title compound was synthesised according to the procedure described for the synthesis of 5-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid (Example S) from 2-Chloro-5-methylsulfamoyl-benzoic acid and rac-3-hydroxy-piperidine and obtained in 15% yield. MS (m/e): 312.9 (MH− 100%).

Aufarbeitung

  1. customobtained in 15% yield

Quellen und Nachweise

ORD-Eintrag
ord-0c38f1143f9b40338d4b171c3d8ea99d
Quelldatensatz
uspto-grants-2009_09
Patentnummer
US07595314B2

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