HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 135737575, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 135735626 | HCID 135735626 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 135737575 | HCID 135737575 | 94% |
Reaction Steps
A suspension of 3.3 g (0.0146 mole) of acetylpyrazolo[1,5-c]quinazolin-5(6H)-one prepared as in part A above in 300 ml of absolute ethanol is cooled to 0° and 2.22 g (0.0584 mole) of sodium borohydride added. Stirring is continued at 0° for fifteen minutes and then at room temperature for 2 hours. The reaction mixture is treated with 150 ml of water, the solution stripped to about 100 ml, saturated with solid sodium chloride and adjusted to pH 6.0 (paper) with dilute (1N) hydrochloric acid. The resultant precipitate is filtered and dried to give 3.1 g of product (94%) melting at 242°-245°. Recrystallization from chloroform-methanol gives 3.0 g of the title compound, m.p. 250°-252°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04112096 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-cfbddd5dac844ce5ad3678e2f4a48c91 |
| Source note | uspto-grants-1978_09 |