HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505329Generated: November 2, 2026
Dichloromethane → HCID 178433171, compound
https://huagongshe.com/reaction/505329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Phenoxyethanamine | HCID 15651 | — |
| Reactant | HCID 178503328 | HCID 178503328 | — |
| Catalyst | Hydrogen Peroxide | HCID 784 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178433171 | HCID 178433171 | 47% |
Reaction Steps
8-Bromo-6-chloro-4-methyl-2-methylsulfanyl-3,4-dihydro-quinazoline hydroiodide (141 mg, 0.33 mmol) and 2-phenoxyethyl amine (53.5 mg, 0.39 mmol) were dissolved in acetonitrile (1 ml) and heated to 200° C. in a sealed tube in a microwave oven for 30 minutes. After cooling the reaction was treated with 1N aqueous sodium hydroxide solution, methylene chloride and 5 to 7 drops of 30% aqueous hydrogen peroxide solution. After the reaction has ceased the layers were separated and the aqueous phase was extracted with methylene chloride. The combined organic layers were dried over sodium sulfate, filtered, the solvent was evaporated and the residue was purified by column chromatography (CH2Cl2:MeOH:aq conc NH3=9:1:0.1) to yield the title compound as an off-white solid (60 mg, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781441B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c91c674f21094a928dd3ad36b2a9e099 |
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| Source note | uspto-grants-2010_08 |
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