HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161853Generated: October 29, 2026
3-Chlorobenzaldehyde → HCID 59519059, compound
https://huagongshe.com/reaction/1161853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | HCID 59519042 | HCID 59519042 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59519059 | HCID 59519059 | 60.5% |
Reaction Steps
In a capped 20 mL scintillation vial, a solution of 2-amino-5-bromo-N-(tert-butylcarbamoylmethyl)benzamide (0.65 g, 2.0 mmol), 3-chlorobenzaldehyde (0.27 mL, 2.4 mmol) and catalytic glacial acetic acid (2 drops) in anhydrous ethanol (10 mL) was heated with stirring at 85° C. for 16 h. The resulting white suspension was cooled to room temperature, the white solid collected by suction filtration and washed with cold EtOH to give 2-[6-bromo-2-(3-chlorophenyl)-4-oxo-1,4-dihydro-2H-quinazolin-3-yl]-N-tert-butylacetamide (0.53 g, 1.21 mmol, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820649B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-963c8e6b024f478f8a3151b00e7ca632 |
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| Source note | uspto-grants-2010_10 |
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