HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363758Generated: October 26, 2026
Ammonium Hydroxide → 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline
https://huagongshe.com/reaction/363758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2,4-Diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline | HCID 54072668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline | HCID 54369095 | 8.9% |
Reaction Steps
A solution of 2.8 grams (0.084 mole) of 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline (prepared in Example 2) in 300 mL of methylene chloride was stirred, and 35 mL of 1.0M boron tribromide in methylene chloride was added. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 21 hours. Thin layer chromatographic analysis of the reaction mixture indicated that the reaction was not complete. The reaction mixture was heated at reflux for about 6 hours, then it was allowed to cool to ambient temperature where it was stirred for about 60 hours. After this time, the reaction mixture was poured into 500 mL of ice containing 100 mL of concentrated ammonium hydroxide. The mixture was filtered to collect a solid. The solid was washed with water and dried at 70° C. under reduced pressure, yielding 2.4 grams of 2,4-diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05874579 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-9811d61b809b425d97ebcd15891545a7 |
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| Source note | uspto-grants-1999_02 |
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