HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate → (Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate | HCID 1480574 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanol | HCID 2736621 | — |
Reaction Steps
To a stirred slurry of LiAlH4 (2.0 g, excess) in dry THF, ethyl imidazo[2,1-b]-benzthiazole-2-carboxylate (4.9 g, 20 mmol) was slowly added in THF (100 ml) at 0° C. After the addition, the reaction mixture was stirred at room temperature for 1 h and quenched with saturated NH4Cl/NH4OH. The separated solid was diluted with Chloroform/MeOH (3:1) and filtered through a pad of celite. The organic layer was washed once with saturated NaCl and dried over anhydrous MgSO4. It was filtered and concentrated. The brown solid obtained was taken to next step with out purification. Yield: 3.8 g, 93%; M+H 205; mp 131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691842B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-ff51e18a5b32430c83d6930fa1121870 |
| Source note | uspto-grants-2010_04 |