HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925992Generated: October 28, 2026
3-Chloro-4-(3-fluorobenzyloxy)aniline → HCID 57597182, compound
https://huagongshe.com/reaction/1925992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-4-(3-fluorobenzyloxy)aniline | HCID 7059263 | — |
| Reactant | Benzoic acid, 3-[(4-chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)methyl]-, methyl ester | HCID 86615755 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 57597182 | HCID 57597182 | 89.6% |
Reaction Steps
To a solution of methyl 3-[(4-chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)methyl]benzoate (670 mg) in 1-methyl-2-pyrrolidone (3.0 mL) was added 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (549 mg), and the reaction mixture was stirred at 120° C. for 1.5 hrs. The reaction mixture was allowed to cool to room temperature, diluted with 5% aqueous sodium hydrogen carbonate solution (50 mL), and extracted with ethyl acetate (50 mL×3). The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (basic silica gel, eluent:hexane/ethyl acetate=9/1→0/10). The object fraction was concentrated under reduced pressure and dried to give the title compound (1010 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178543B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-9656591ca5f64270b166c52d61cdd979 |
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| Source note | uspto-grants-2012_05 |
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