HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594936Generated: October 31, 2026
o-Fluorobenzaldehyde → HCID 86689211, compound
https://huagongshe.com/reaction/594936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 86689212 | HCID 86689212 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86689211 | HCID 86689211 | — |
Reaction Steps
In a flask, dichloromethane (0.295 mL) and acetic acid (2 drops) was added to N-(piperidin-3-yl)-3-(pyridin-4-yl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxamide trifluoroacetate salt (0.021 g, 0.05 mmol) and 2-fluorobenzaldehyde (0.0124 g, 0.1 mmol). The reaction was sonicated for 1 hr. Sodium triacetoxyborohydride (0.050 g, 0.25 mmol) was added in one portion. The reaction was stirred for an additional 16 hours. Saturated sodium bicarbarbonate (1 mL) was added. The reaction was stirred for an additional 5 minutes and was extracted with dichloromethane (3×1 mL). The extracts were combined, dried with anhydrous sodium sulfate, filtered, and concentrated in vacuo. The resulting crude product was purified by prep LC/MS. LC-MS: 435.68 [M+H]. LC/MS RT=1.82 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242981B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-0b233736ecec4724b6d0450a838e663f |
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| Source note | uspto-grants-2016_01 |
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