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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423006Generated: October 31, 2026

Benzenamine, 3-ethynyl- → HCID 16733971, compound

https://huagongshe.com/reaction/2423006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactant6,7-Diacetoxy-4-chloro-quinazolineHCID 27281377—
ProductHCID 16733971HCID 1673397179%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

Into a 2.0 Lt four-necked round-bottomed flask, equipped with a mechanical stirrer, reflux condenser and thermometer socket are charged the organic layer from the previous stage (Step 3) containing 4-Chloro-6,7-diacetoxy-quinazoline and 3-ethynylaniline (20 g). The reaction mass was slowly heated to reach reflux condition and maintained and reflux for 14 hours and the reaction was found to be over by HPLC. Then the reaction was cooled to 25-30° C. and filtered the mass washed the cake with chloroform and dried to get 60 g (79% by theory) of N-(3-ethynylphenyl)-6,7-diacetoxy-4-quinazolinamine hydrochloride as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960545B2
Source datasetuspto-grants-2011_06
ORD IDord-a925205702f2470e9ecdfd9ba66ec60f
Source noteuspto-grants-2011_06