Hydrochloric Acid → N-(2-Fluoro-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide Hydrochloride

HRID 335273Notes

Reaction equation

HRID 335273 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:24])[NH:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N:17]2[CH2:22][CH2:21][N:20]([CH3:23])[CH2:19][CH2:18]2)=[CH:4][C:3]=1[NH:25][C:26]([C:28]1[N:32]2[CH:33]=[CH:34][C:35]([C:37]3[CH:38]=[N:39][N:40]([CH3:42])[CH:41]=3)=[CH:36][C:31]2=[N:30][CH:29]=1)=[O:27].[ClH:43].CCOCC>CO>[ClH:43].[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:24])[NH:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N:17]2[CH2:18][CH2:19][N:20]([CH3:23])[CH2:21][CH2:22]2)=[CH:4][C:3]=1[NH:25][C:26]([C:28]1[N:32]2[CH:33]=[CH:34][C:35]([C:37]3[CH:38]=[N:39][N:40]([CH3:42])[CH:41]=3)=[CH:36][C:31]2=[N:30][CH:29]=1)=[O:27]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 71283574N-(2-Fluoro-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide

Product 1

HCID 71283573N-(2-Fluoro-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide Hydrochloride

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

N-(2-Fluoro-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide (step 1) (30 mg, 0.053 mmol) in MeOH (2 ml) was treated with HCl in ether (0.053 ml, 0.053 mmol) and the solution was evaporated to dryness and dried in vacuo overnight to afford the title compound; LC-MS: Rt 0.82 mins; MS m/z 56, [M+H]+; Method 2minLC_v003

Workup

  1. customthe solution was evaporated to dryness
  2. customdried in vacuo overnight

Sources & evidence

ORD record
ord-573141bdfa3a46c8acb57a6be854b3f4
Source dataset
uspto-grants-2014_11
Patent number
US08883819B2

Reaction notes

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