HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690980Generated: October 25, 2026
Sodium hydride → 3-(1-(3-Phenoxy-benzyl)-1H-pyrazol-4-yl)-pyridin-2-ylamine
https://huagongshe.com/reaction/1690980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Phenoxybenzyl chloride | HCID 93291 | — |
| Reactant | 3-(1H-pyrazol-4-yl)-pyridin-2-ylamine | HCID 59255290 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(1-(3-Phenoxy-benzyl)-1H-pyrazol-4-yl)-pyridin-2-ylamine | HCID 59255136 | 47% |
Reaction Steps
To a solution of 3-(1H-pyrazol-4-yl)-pyridin-2-ylamine (20 mg, 0.13 mmol) described in Manufacturing Example 32-1-4 in N,N-dimethylformamide (10 mL) was added sodium hydride (7.5 mg, 0.19 mmol, 60% in oil) under nitrogen atmosphere on an ice bath (0° C.), which was stirred for 40 minutes at room temperature. 1-Chloromethyl-3-phenoxybenzene (32.8 mg, 0.15 mmol) described in Manufacturing Example 35-1-1 was then added and stirred for 30 minutes at room temperature. The reaction mixture was partitioned into water and ethyl acetate at room temperature. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=2:1, then ethyl acetate only) to obtain the title compound (20 mg, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153662B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-2d6368eba7c54811b1b71abab002050c |
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| Source note | uspto-grants-2012_04 |
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