(4-Benzylpiperidin-1-yl)oxoacetic acid → HCID 69101021, compound

HRID 2114999Notes

Reaction equation

HRID 2114999 reaction equation
[CH2:1]([CH:8]1[CH2:13][CH2:12][N:11]([C:14](=[O:18])[C:15]([OH:17])=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:19][C:20]1[CH:21]=[CH:22][C:23]2[NH:27][S:26](=[O:29])(=[O:28])[CH2:25][C:24]=2[CH:30]=1>>[CH2:1]([CH:8]1[CH2:9][CH2:10][N:11]([C:14](=[O:18])[C:15]([NH:19][C:20]2[CH:21]=[CH:22][C:23]3[NH:27][S:26](=[O:29])(=[O:28])[CH2:25][C:24]=3[CH:30]=2)=[O:17])[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 16110264(4-Benzylpiperidin-1-yl)oxoacetic acidHCID 217951445-Amino-1,3-dihydrobenzo[c]isothiazole 2,2-dioxide

Product 1

HCID 69101021HCID 69101021, compound

Procedure

The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and 5-amino-1,3-dihydro-2,1-benzisothiazole-2,2-dioxide [J. Het. Chem., 23, 1645. (1986)] according to the method described in Example 2. The filtered crystals are purified by column chromatography using Kieselgel 60 (Merck) as adsorbent and toluene:methanol=4:1 as eluent. Melting Point: 181-182° C. (isopropanol)

Workup

  1. customThe filtered crystals are purified by column chromatography

Sources & evidence

ORD record
ord-33cc5e72edc041c392b2df9c3096fe1d
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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