HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44604Generated: October 25, 2026
Ethyl 8-[(aminocarbonyl)amino]-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate → 8-[(aminocarbonyl)amino]-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide
https://huagongshe.com/reaction/44604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 8-[(aminocarbonyl)amino]-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate | HCID 68932803 | — |
| Reactant | Methanol dimethylformamide ammonium hydroxide | HCID 86614109 | — |
| Product | 8-[(aminocarbonyl)amino]-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide | HCID 68937962 | 50% |
Reaction Steps
A suspension of 0.20 g (0.63 mmol) of ethyl 8-[(aminocarbonyl)amino]-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate in 15 mL of a mixture methanol/dimethylformamide/ammonium hydroxide 30% 1/1/1 was stirred in a close bottle at 65° C. for 48 hours. The solvent was then evaporated under reduced pressure, the residue redissolved with a mixture dichloromethane/methanol 9/1 and washed with water. The organic layer was dried over anhydrous Na2SO4 and evaporated to dryness. The product was purified by chromatography on a silica gel column (eluant dichloromethane/acetone/methanol) giving 0.09 g (50% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541429B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-16bcced8852b40dcb88c9f5fc4b2c558 |
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| Source note | uspto-grants-2013_09 |
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