HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640005Generated: October 31, 2026
7-(Benzyloxy)-4-chloroquinazoline → 2-(4-{[7-(benzyloxy)quinazolin-4-yl]amino}-1H-pyrazol-1-yl)-N-(3-fluorophenyl)acetamide hydrochloride
https://huagongshe.com/reaction/640005
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-(Benzyloxy)-4-chloroquinazoline | HCID 22030923 | — |
| Reactant | 2-(4-amino-1H-pyrazol-1-yl)-N-(3-fluorophenyl)acetamide | HCID 28374007 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-(4-{[7-(benzyloxy)quinazolin-4-yl]amino}-1H-pyrazol-1-yl)-N-(3-fluorophenyl)acetamide hydrochloride | HCID 68639095 | 82% |
Reaction Steps
A mixture of 7-(benzyloxy)-4-chloroquinazoline (1.94 g, 7.17 mmol) and 2-(4-amino-1H-pyrazol-1-yl)-N-(3-fluorophenyl)acetamide (1.66 g, 7.09 mmol) in dimethylacetamide (25 ml) was heated at 90° C. for 1 hour. The mixture was cooled to room temperature and then diluted with diethyl ether (75 ml) and filtered. The solid was washed with diethyl ether and dried to yield 2-(4-{[7-(benzyloxy)quinazolin-4-yl]amino}-1H-pyrazol-1-yl)-N-(3-fluorophenyl)acetamide hydrochloride (2.92 g, 82% yield) as a yellow solid:
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-a03ec6f5ef9649998411dd565e408ab9 |
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| Source note | uspto-grants-2010_04 |
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