4-(Benzthiazole-2-carbonyl)piperidine → N-methyl-N-(4-(4-(benzthiazole-2-carbonyl)piperidin-1-yl)-2-(3,4-dichlorophenyl)butyl)benzamide

HRID 379448Notes

Reaction equation

HRID 379448 reaction equation
[CH3:1][N:2]([CH2:11][CH:12]([C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[C:21]([Cl:26])[CH:20]=1)[CH2:13][CH2:14]S(C)(=O)=O)[C:3](=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[S:27]1[C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=2[N:29]=[C:28]1[C:36]([CH:38]1[CH2:43][CH2:42][NH:41][CH2:40][CH2:39]1)=[O:37]>>[CH3:1][N:2]([CH2:11][CH:12]([C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[C:21]([Cl:26])[CH:20]=1)[CH2:13][CH2:14][N:41]1[CH2:42][CH2:43][CH:38]([C:36]([C:28]2[S:27][C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=3[N:29]=2)=[O:37])[CH2:39][CH2:40]1)[C:3](=[O:10])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1

Participants

3

Reactant 2

HCID 152370094-(Benzthiazole-2-carbonyl)piperidineHCID 18354486N-methyl-N-(2-(3,4-dichlorophenyl)-4-methanesulfonylbutyl)benzamide

Product 1

HCID 10120994N-methyl-N-(4-(4-(benzthiazole-2-carbonyl)piperidin-1-yl)-2-(3,4-dichlorophenyl)butyl)benzamide

Procedure

Prepare by the method of Example 2.7 using N-methyl-N-(2-(3,4-dichlorophenyl)-4-methanesulfonylbutyl)benzamide and 4-(benzthiazole-2-carbonyl)piperidine to give the title compound.

Sources & evidence

ORD record
ord-8c0a90dcb30149d293990bd3a752521f
Source dataset
uspto-grants-2001_10
Patent number
US06297259B1

Reaction notes

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