HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614551Generated: October 26, 2026
Methanol → 2-(Hydroxymethyl)pyrazolo(1,5-c)quinazolin-5(6H)-one
https://huagongshe.com/reaction/614551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 5,6-Dihydro-5-oxopyrazolo[1,5-c]quinazoline-2-carboxylic acid ethyl ester | HCID 136023344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(Hydroxymethyl)pyrazolo(1,5-c)quinazolin-5(6H)-one | HCID 135449340 | 99.1% |
Reaction Steps
A suspension of 3.84 g (0.015 mole) of 5,6-dihydro-5-oxopyrazolo[1,5-c]quinazoline-2-carboxylic acid ethyl ester prepared as described in part A above is stirred in 150 ml of tetrahydrofuran under nitrogen at room temperature. There is added 24 ml (0.034 mole) of a 20% solution of diisobutyl aluminum hydride in hexane. The resultant solution is stirred for 1 hour at room temperature whereupon 50 ml of methanol is added and the reaction mixture refluxed for 1 hour. The precipitate of aluminum alkoxide is filtered, air dried and Soxhlet extracted for 48 hours with boiling methanol. The extract is combined with the above filtrate and stripped to give 3.2 g of a white solid (quantitative yield). Recrystallization from methanol gives 2.7 g of pure title compound, m.p. 285°-287°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04145420 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-1250957b1fde4157add8598c644ccc16 |
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| Source note | uspto-grants-1979_03 |
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