HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754791Generated: October 28, 2026
Potassium Hydroxide → (5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-[2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazol-3-yl]-methanone
https://huagongshe.com/reaction/1754791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 24229213 | — |
| Reactant | 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehyde | HCID 57619207 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-[2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazol-3-yl]-methanone | HCID 24954284 | 2.1% |
Reaction Steps
5-Chloro-1H-pyrrolo[2,3-b]pyridine (532, 0.068 g, 0.44 mmol) was combined with methanol (10 mL) and potassium hydroxide (0.16 g, 2.8 mmol). The mixture was stirred for 50 minutes, then 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehyde (530, 0.100 g, 0.40 mmol, prepared as described in Example 47, Scheme 162, Step 5) was added and the reaction was stirred overnight at room temperature and then concentrated. Ethyl acetate was added and the mixture was washed with sodium bicarbonate saturated solution and brine. After drying over anhydrous sodium sulfate the solvent was removed under reduced pressure. Purification with silica gel column chromatography eluting with a gradient of ethyl acetate (10-100%) in hexanes provided the desired compound (0.0033 g, 2%). MS (ESI) [M+H+]+=398.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169250B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-6439884a824d424692cff7de86ccc010 |
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| Source note | uspto-grants-2015_10 |
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