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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377072Generated: October 30, 2026

Hydrochloric Acid → 1-[(4-fluorophenyl)methyl]-N-hydroxy-N-methyl-pyrazolo[3,4-c]pyridine-5-carboxamide

https://huagongshe.com/reaction/2377072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantTriethylamineHCID 8471—
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantMethyl 1H-pyrazolo[3,4-C]pyridine-5-carboxylateHCID 59855813—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-[(4-fluorophenyl)methyl]-N-hydroxy-N-methyl-pyrazolo[3,4-c]pyridine-5-carboxamideHCID 15957053100%

Reaction Steps

To a stirring solution of methyl 1H-pyrazolo[3,4-c]pyridine-5-carboxylate (100 mg, 0.351 mmol) in methanol (4 mL) was added a 3.0 M solution of LiOH in water (0.351 mL, 1.05 mmol) and the mixture was stirred overnight, then 1.0 M hydrochloric acid in diethyl ether was added (1.05 mL, 1.05 mmol) and the solvent was evaporated under reduced pressure. The crude solid was dissolved in DMF and N-methylhydroxylamine hydrochloride (58 mg, 0.698 mmol) was added followed by triethylamine (214 mL, 1.154 mmol) and HATU (266 mg, 0.698 mmol). The mixture was stirred overnight. Water was added and the mixture was extracted with dichloromethane (3×20 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The crude solid was dissolved in DMSO and purified by reverse phase preparative HPLC to provide a white solid (105 mg, 100% yield). 1H NMR (DMSO-d6): & 10.24 (bs, 1H), 9.26 (s, 1H), 8.07 (s, 1H), 7.37 (m, 2H), 7.15 (m, 2H), 5.81 (s, 2H), 3.31 (s, 3H). Anal. HPLC: >95% (@ 254, 222 nM). HRMS calcd for C15H13FN4O2 (M+H) 301.1088, found 301.1096.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468375B2
Source datasetuspto-grants-2008_12
ORD IDord-6166b0edfa184ecca3bd6dfd6bcccd09
Source noteuspto-grants-2008_12