HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360502Generated: November 2, 2026
Isopropyl isocyanate → HCID 57717573, compound
https://huagongshe.com/reaction/1360502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl isocyanate | HCID 61277 | — |
| Reactant | HCID 57717565 | HCID 57717565 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57717573 | HCID 57717573 | 11.3% |
Reaction Steps
Isopropyl isocyanate (255 mg, 3.00 mmol) was added to a 0° C. stirred solution of 1-(2-amino-2-methylpropyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-amine (prepared as described in Example 64, 892 mg, 3.00 mmol) in dichloromethane (26.7 mL). After 4 hours at 0° C., the solution was stirred overnight at ambient temperature. The solution was concentrated to afford a colorless resin that was purified by IFC (silica gel, elution with CMA in chloroform). The appropriate fractions were combined and concentrated to yield a solid that was recrystallized from ethyl acetate in hexanes. The solid was isolated by filtration, washed with ethyl acetate/hexanes, and dried to yield 130 mg of N-[2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)-1,1-dimethylethyl]-N′-isopropylurea as a white solid, mp 190-191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879849B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-b458df629a214bd8beac48c5bc26b838 |
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| Source note | uspto-grants-2011_02 |
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