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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Methyl 1H-pyrazolo[3,4-C]pyridine-5-carboxylate | HCID 59855813 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[(4-fluorophenyl)methyl]-N-hydroxy-N-methyl-pyrazolo[3,4-c]pyridine-5-carboxamide | HCID 15957053 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468375B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-6166b0edfa184ecca3bd6dfd6bcccd09 |
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| Source note | uspto-grants-2008_12 |
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