Potassium Carbonate → HCID 178513542, compound

HRID 1888266Notes

Reaction equation

HRID 1888266 reaction equation
Cl[CH2:2][CH2:3][CH2:4][S:5]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:22]3[C:17](=[C:18]([C:30]([NH2:32])=[O:31])[CH:19]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=4)[CH:21]=3)[NH:16][N:15]=2)[CH2:10][CH2:9]1)(=[O:7])=[O:6].C([O-])([O-])=O.[K+].[K+].[N:39]1([CH:45]2[CH2:50][CH2:49][NH:48][CH2:47][CH2:46]2)[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]1>CN(C=O)C>[N:39]1([CH:45]2[CH2:50][CH2:49][N:48]([CH2:2][CH2:3][CH2:4][S:5]([N:8]3[CH2:13][CH2:12][CH:11]([C:14]4[C:22]5[C:17](=[C:18]([C:30]([NH2:32])=[O:31])[CH:19]=[C:20]([C:23]6[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=6)[CH:21]=5)[NH:16][N:15]=4)[CH2:10][CH2:9]3)(=[O:7])=[O:6])[CH2:47][CH2:46]2)[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 786071,4'-BipiperidineHCID 1785135403-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-(3-fluorophenyl)-1H-indazole-7-carboxamide

Product 1

HCID 178513542HCID 178513542, compoundYield 39.2%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

The title compound was prepared according to the general procedure of Example 38b. Thus, 3-{1-[(3-Chloropropyl)sulfonyl]-4-piperidinyl}-5-(3-fluorophenyl)-1H-indazole-7-carboxamide (Example 38a) (0.222 mmol) in DMF (4 mL) was reacted with K2CO3 (61 mg, 0.444 mmol) and 4-piperidino-piperidine (187 mg, 1.11 mmol) to afford the title compound (53.14 mg, 39% for 2 steps).

Workup

  1. customThe title compound was prepared

Sources & evidence

ORD record
ord-a4f812507905436faf2b67cb2da8ed10
Source dataset
uspto-grants-2013_08
Patent number
US08501780B2

Reaction notes

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