HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354856Generated: October 25, 2026
Pyridine → 4-Amino-6-(2-ethylbutyramido)quinazoline
https://huagongshe.com/reaction/354856
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Tripropylamine | HCID 7616 | — |
| Reactant | 2-Ethylbutyryl chloride | HCID 75954 | — |
| Reactant | 4,6-Diaminoquinazoline hydrochloride | HCID 20266086 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Amino-6-(2-ethylbutyramido)quinazoline | HCID 13060462 | 46.4% |
Reaction Steps
To a mixture of 4,6-diaminoquinazoline hydrochloride (1.97 g), tripropylamine (2.60 g) and dry pyridine (20 ml) in an ice-bath was added dropwise during 10 minutes 2-ethylbutyryl chloride (1.75 g). The mixture was stirred for 3 hours at the same temperature. Crushed ice was added to the reaction mixture. The mixture was stirred for 5 minutes and concentrated under reduced pressure. After the addition of water (50 ml), sodium hydrogen carbonate (3.36 g) was added in small portions to the residue to give precipitates which were separated by filtration, washed with water and dried. The crude crystals were dissolved in a mixture of chloroform and methanol under heating. After insoluble materials were removed by filtration, the filtrate was concentrated under reduced pressure to give a residue, which was suspended in ethyl acetate. After stirring under heating, the suspension was filtered to give crystalline 4-amino-6-(2-ethylbutyramido)quinazoline (1.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377580 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-ae43a9f70ec44aebbc425fc972d2f400 |
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| Source note | uspto-grants-1983_03 |
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