HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916458Generated: October 30, 2026
4-Chloro-7-methoxyquinazolin-6-yl acetate → 4-Chloro-7-methoxyquinazolin-6-ol
https://huagongshe.com/reaction/916458
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-7-methoxyquinazolin-6-yl acetate | HCID 22022160 | — |
| Solvent | Ammonia | HCID 222 | — |
| Product | 4-Chloro-7-methoxyquinazolin-6-ol | HCID 23132475 | 67.8% |
Reaction Steps
6-Acetoxy-4-chloro-7-methoxyquinazoline (10.0 g, 39.6 mmol), (WO 01/04102, Table VI examples), was added in portions to a stirred 7N methanolic ammonia solution (220 ml) and the mixture cooled to 10° C. in an ice/water bath. Initially the solid dissolved to give a yellow solution which then deposited a yellow precipitate. After stirring for one hour the precipitate was filtered off, washed with diethyl ether and dried thoroughly under high vacuum to give 4-chloro-6-hydroxy-7-methoxyquinazoline (5.65 g, 67.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268230B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-dabbb77dc4ee4de6a88378da173b268a |
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| Source note | uspto-grants-2007_09 |
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