HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495435Generated: October 31, 2026
Ammonia → 5-Quinazolinol, 2-methyl- (9CI)
https://huagongshe.com/reaction/495435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 22326675 | HCID 22326675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Quinazolinol, 2-methyl- (9CI) | HCID 135553017 | 15% |
Reaction Steps
To a stirred solution of 5-methoxy-2-methylquinazoline (0.22 g, 1.26 mmol) in dichloromethane (20 mL) at 0° C. under argon was added a solution of boron tribromide in dichloromethane (1M, 3.8 mL), dropwise over 0.01 h. The resulting mixture was stirred at 20° C. for 48 h then poured into a mixture of ice (50 g) and 0.880 aqueous ammonia (50 mL) and stirred for 0.5 h. Organic phase was separated and aqueous phase washed with dichloromethane (3×30 mL). The aqueous phase was acidified (pH 6) with citric acid and the resulting mixture extracted with ethyl acetate (3×50 mL). The combined ethyl acetate extracts were dried (Na2SO4) and evaporated in vacuo to give the title compound (0.030 g, 15%) as an oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06939871B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-ae96c8d7b03a4c9d8cb11f8d2ac0841b |
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| Source note | uspto-grants-2005_09 |
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