HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423005Generated: October 29, 2026
Chloroform → 4-Chloroquinazoline-6,7-diyl diacetate
https://huagongshe.com/reaction/2423005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 136013901 | HCID 136013901 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloroquinazoline-6,7-diyl diacetate | HCID 27281377 | — |
Reaction Steps
Into a 3.0 L four necked round bottomed flask, equipped with a mechanical stirrer, reflux condenser, pressure equalizing addition funnel and thermometer socket are charged chloroform (1000 ml), 6,7-diacetoxy-4(3H)-quinazolinone (50 g) obtained by the process described in step (ii) above and dimethylformamide (2 ml). Oxalyl chloride (50 g) was slowly added in about 20-30 minutes. The reaction mass was slowly heated to reflux temperature and maintained at reflux temperature for 6 hours. Reaction was found to be over by HPLC. Cooled the reaction mass to 25-30° C. and slowly quenched into saturated sodium bicarbonate solution at less than 10° C. Separated the organic layer and dried over anhydrous sodium sulfate. The dried organic layer thus obtained was directly used in the next step without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960545B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-1589c0cbaf6e464e92e1365ed6d00238 |
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| Source note | uspto-grants-2011_06 |
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