Hydrochloric Acid → HCID 178434397, compound
Reaction equation
[CH3:1][C:2]1([NH:8][C:9]([C:11]2[C:12]3[C:26]([CH3:27])=[N:25][N:24](C4CCCCO4)[C:13]=3[N:14]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=3)[CH:16]=2)=[O:10])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.Cl>C1COCC1>[CH3:1][C:2]1([NH:8][C:9]([C:11]2[C:12]3[C:26]([CH3:27])=[N:25][NH:24][C:13]=3[N:14]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=3)[CH:16]=2)=[O:10])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 6-(4-hydroxy-phenyl)-3-methyl-1-(tetrahydro-pyran-2-yl)-1H-pyrazolo-[3,4-b]pyridine-4-carboxylic acid (4-methyl-piperidin-4-yl)-amide (75 mg) in THF (1 mL) was added to a stirred solution of HCl (4N in dioxane). The mixture was stirred at r.t. overnight, the precipitate formed was filtered off and washed with ethyl acetate and acetone and dried in air to give 72 mg (99%) of the title compound as hydrochloride
Workup
- customthe precipitate formed
- filtrationwas filtered off
- washwashed with ethyl acetate and acetone
- customdried in air
Sources & evidence
- ORD record
- ord-013566ac2b2a45b3b71b057b2fd9f1a5
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686150B2
Reaction notes
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