HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(Hydroxyphenylmethyl)pyrazolo[1,5-c]quinazolin-5(6H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Benzoylpyrazolo[1,5-c]quinazolin-5(6H)-one | HCID 135737590 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Hydroxyphenylmethyl)pyrazolo[1,5-c]quinazolin-5(6H)-one | HCID 135737591 | — |
Reaction Steps
1.65 g 80.0057 mole) of 2-benzoylpyrazolo[1,5-c]-quinazolin-5(6H)-one prepared as in part B above is stirred with 880 mg (4 equiv) of sodium borohydride in absolute ethanol (125 ml) at room temperature for 3 hours. The reaction mixture is stripped to dryness and the resulting solid is suspended in water (40 ml), cooled down to 0° and treated dropwise with 1 N HCl 25 ml). The mixture is stirred for 30 minutes, diluted with water (40 ml) and stirred for another 10 minutes. The white precipitates are filtered off, washed well with water and dried overnight in a vacuum oven at 70° C to give 1.6 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04076818 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-b65d70e31af048b0bde2c0e6b3ee36a0 |
| Source note | uspto-grants-1978_02 |