HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639983Generated: October 29, 2026
Phosphorus oxychloride → N-(2,3-difluorophenyl)-2-{4-[(7-hydroxy-5-isopropoxyquinazolin-4-yl)amino]-1H-pyrazol-1-yl}acetamide
https://huagongshe.com/reaction/639983
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(4-amino-1H-pyrazol-1-yl)-N-(2,3-difluorophenyl)acetamide | HCID 16067954 | — |
| Reactant | 7-Acetoxy-5-isopropoxy-3,4-dihydroquinazolin-4-one | HCID 135510705 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,3-difluorophenyl)-2-{4-[(7-hydroxy-5-isopropoxyquinazolin-4-yl)amino]-1H-pyrazol-1-yl}acetamide | HCID 136383489 | 60% |
Reaction Steps
Phosphoryl chloride (3.7 ml, 40 mmol) was added to a solution of 5-isopropoxy-4-oxo-3,4-dihydroquinazolin-7-yl acetate (2.6 g, 10 mmol) and di-iso-propylethylamine (14 ml, 80 mmol) in 1,2-dichloroethane (75 ml) and the reaction was heated at 80° C. for 1 hour. The mixture was evaporated under reduced pressure and the residue suspended in dimethylacetamide (30 ml). 2-(4-Amino-1H-pyrazol-1-yl)-N-(2,3-difluorophenyl)acetamide (2.5 g, 10 mmol) was added and the mixture was then heated at 90° C. for 1 hour. The mixture was evaporated under reduced pressure and the residue stirred in a 7N solution of ammonia in methanol (100 ml) at ambient temperature for 2 hours. The mixture was evaporated under reduced pressure to leave a yellow solid which was stirred in water (50 ml) for 1 hour, then filtered and the residue purified by silica gel chromatography eluting with a 0 to 10% mixture of methanol in dichloromethane to give N-(2,3-difluorophenyl)-2-{4-[(7-hydroxy-5-isopropoxyquinazolin-4-yl)amino]-1H-pyrazol-1-yl}acetamide (2.7 g, 60% yield):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691867B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-dbf6f1c1973f4a1899b213b5bff33d39 |
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| Source note | uspto-grants-2010_04 |
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