HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15521023, compound → 2,3-Dimethylimidazo[2,1-b]thiazole-5-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15521023 | HCID 15521023 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Dimethylimidazo[2,1-b]thiazole-5-methanol | HCID 15521024 | — |
Reaction Steps
A solution of 2,3-Dimethylimidazo[2,1-b]thiazole-5-carboxylic acid ethyl ester (Formula A-4) (1.68 g) in THF (50 mL) at 0° was treated with LiAlH4 (0.38 g) and reacted at 25° for 1.5 hours. Excess reagent was quenched by sequential addition of water and 15% sodium hydroxide. The resulting mixture was diluted with THF (100 mL), filtered, and the filtrate was evaporated to a residue of crude 2,3-Dimethylimidazo[2,1-b]thiazole-5-methanol (Formula A-5) (1.04 g). Crystallization from isopropanol solution gave pure 2,3-Dimethylimidazo[2,1-b]thiazole-5-methanol (Formula A-5), m.p. 166-167°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191124B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-4364517fd43d499294f13f4448b543d5 |
| Source note | uspto-grants-2001_02 |