2-Benzylpiperidin-4-one → 6-Benzyl-5-(4-chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

HRID 15748Notes

Reaction equation

HRID 15748 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:16](C3C=CC=CC=3)[CH2:15][C:14]3=[N:23][NH:24][CH:25]=[C:13]3[CH2:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[C:26]1([CH2:32]C2CC(=O)CCN2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[CH2:32]([CH:16]1[N:11]([S:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)(=[O:10])=[O:9])[CH2:12][C:13]2[CH:25]=[N:24][NH:23][C:14]=2[CH2:15]1)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Participants

3

Procedure

Prepared as described for compound 55 in Example 1 using 2-(phenylmethyl)-4-piperidinone.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-d3ed59c7bd904a10b684b402ea0671cc
Source dataset
uspto-grants-2010_06
Patent number
US07732609B2

Reaction notes

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