HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296449Generated: October 29, 2026
Pyridine → Diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioate
https://huagongshe.com/reaction/2296449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diethyl[(6-amino-4-quinazolinylamino)methylene]propanedioate | HCID 20266113 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioate | HCID 13060488 | 64.4% |
Reaction Steps
A mixture of diethyl [(6-amino-4-quinazolinylamino)methylene]propanedioate (3.03 g), pyridine (3.63 g) and dichloromethane (93 ml) was ice-cooled. To the mixture was added acetic anhydride (1.88 g). The reaction mixture was stirred for 30 minutes under ice-cooling and then for 2 hours and 15 minutes at ambient temperature. Ice water was added to the mixture. The resultant mixture was extracted with chloroform. The organic layer was washed three times with water and with aqueous solution saturated with sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a residue, which was purified by a column chromatography on silica gel (developing solvent: chloroform) and recrystallized from chloroform, ethyl acetate and hexane to give crystalline diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioate (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04429126 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-36de197c0f3f4c6eb322034383523250 |
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| Source note | uspto-grants-1984_01 |
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