HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-(cyclohexylamino)-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide → Diethyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-(cyclohexylamino)-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide | HCID 11652736 | — |
| Reactant | Ethyl 8-{[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]amino}-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate | HCID 57444099 | — |
| Product | Diethyl Ether | HCID 3283 | 829.5% |
| Product | Ethyl 1-methyl-8-(pyrrolidin-3-ylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate | HCID 68958913 | — |
Reaction Steps
A solution of 110 mg (0.27 mmol) of ethyl 8-{[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]amino}-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate in a mixture dichoromethane-trifluoroacetic acid 9/1 was stirred at room temperature for 6 hours. The solvent was then removed in vacuo and the resulting oil taken up with dichloromethane and washed with aqueous NaHCO3. The organic layer was dried over Na2SO4 and evaporated. The residue was triturated with diethylether giving 83 mg (60% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482354B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-334455adbb464d2fb2993ddd8336beb4 |
| Source note | uspto-grants-2009_01 |