Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | HCID 178487377 | HCID 178487377 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14822480 | HCID 14822480 | 35.2% |
Reaction Steps
A mixture of 17.1 g 7-methoxy-1H-pyrazolo[3,4-b]quinolin-3-amine (Example 3d), 15.25 g 4-(2-chloroethyl)morpholine hydrochloride, 7.2 g sodium hydride and 500 ml dimethylformamide was stirred at room temperature for about 16 hours. The solvent was then removed by evaporation, and the residue dissolved in 1N hydrochloric acid and extracted with ethyl acetate. The aqueous layer was made basic with carbonate to pH 8 and extracted with chloroform. The chloroform extracts were washed with water, dried over magnesium sulfate and passed through a silica gel pad. The pad was eluted with warm ethyl acetate, the product isolated and recrystallized from ethyl acetate to give 9.2 g 7-methoxy-1-[2-(4-morpholinyl)ethyl]-1H-pyrazolo[3,4-b]quinolin-3-amine, orange solid, m.p. 166°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04920128 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-7cd319e2dd0c4749bc8ec3717d88390f |
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| Source note | uspto-grants-1990_04 |
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