HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl-7-chloroimidazo(2,1-b)benzothiazole-2-carboxylate → HCID 11218645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl-7-chloroimidazo(2,1-b)benzothiazole-2-carboxylate | HCID 396584 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | HCID 11218645 | HCID 11218645 | 72% |
Reaction Steps
7-chloro imidazo[2,1-b]-benzthiazole-2-methanol was prepared according to the procedure outlined in Example 1, (Step 2). Starting from ethyl 7-chloroimidazo[2,1-b]-benzthiazole-2-carboxylate (9.0 g, 32.1 mmol) and LiAlH4 (4.0 g, excess), 5.5 g (72% yield) of the alcohol derivative was isolated as brown solid. mp 166° C. (M+H) 239.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691842B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-9dff3562e835446ab99397b7cc475e68 |
| Source note | uspto-grants-2010_04 |