HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737477Generated: October 30, 2026
7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochloride → 7-Benzyloxy-6-methoxy-4-phenoxyquinazoline
https://huagongshe.com/reaction/1737477
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochloride | HCID 22030836 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Benzyloxy-6-methoxy-4-phenoxyquinazoline | HCID 21874814 | 190% |
Reaction Steps
7-Benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (1.6 g, 4.7 mmol), (prepared as described for the starting material in Example 1), was then added and the reaction mixture heated at 110° C. for 2 hours. The mixture was allowed to cool, water was added and the mixture extracted with ethyl acetate (3×100 ml). The combined extracts were then washed with 2M sodium hydroxide solution, water and brine. Removal of the solvent under reduced pressure gave 7-benzyloxy-6-methoxy-4-phenoxyquinazoline (1.6 g, 95%) as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962458 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-1fdb6890c9df46f3b146593741213f7f |
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| Source note | uspto-grants-1999_10 |
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