HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 467102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (2-Phenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanone | HCID 57013581 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 467102 | HCID 467102 | 86.9% |
Reaction Steps
A solution of (2-Phenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanone (Formula B-6) (0.40 g) in ethanol (5.0 mL) was treated with a solution of NaBH4 (0.05 g) in ethanol (5 mL) and reacted for 18 hours. The solvent was removed in vacuo and the residue was treated with 5% acetic acid solution. Precipitated 3-Methyl-α-(2-phenylethyl)imidazo[2,1-b]thiazole-5-methanol (Formula B-8) (0.38 g) was filtered and recrystallized from isopropanol solution to provide pure 3-Methyl-α-(2-phenylethyl)imidazo[2,1-b]thiazole-5-methanol (Formula B-8) (0.35 g), m.p. 144-145°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191124B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-c8d63c44a6bf4ce8afb4bd9c1c73bfbf |
| Source note | uspto-grants-2001_02 |