HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 20377591, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20377597 | HCID 20377597 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20377591 | HCID 20377591 | — |
| Product | HCID 135737536 | HCID 135737536 | — |
Reaction Steps
To a suspension of 0.28 g of 7-chloro-5-phenylimidazo[1,2-a]quinazoline in 20 ml of ethanol was added 0.2 g of sodium borohydride, and the mixture was heated under reflux for 10 hours. After cooling, the mixture was poured into ice-water, and the resulting precipitate was collected by filtration, washed with water and dried. The product was dissolved in chloroform and absorbed on an activated alumina column. Elution with chloroform and recrystallization from ethanol gave 7-chloro-4,5-dihydro-5-phenylimidazo[1,2-a]quinazoline (m.p. 239°-241° C.) and 7-chloro-1,2,4,5-tetrahydro-5-phenylimidazo[1,2-a]quinazoline (m.p. 210°-213° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183932 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-af6f4344069f4949a76e8ae918c6d899 |
| Source note | uspto-grants-1980_01 |