HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-methylbenzothiazole → Ethyl 7-methylimidazo[2,1-b][1,3]benzothiazole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-methylbenzothiazole | HCID 17335 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Product | Ethyl 7-methylimidazo[2,1-b][1,3]benzothiazole-2-carboxylate | HCID 638597 | 57.6% |
Reaction Steps
Ethyl 7-methylimidazo[2,1-b]-benzthiazole-2-carboxylate was prepared according to the procedure as outlined in Example 1, (Step 1). Starting from 6-methyl-2-amino benzothiazole (3.2 g, 20 mmol) and ethyl bromopyruvate (4.0 g, 20.4 mmol), 3.0 g (57% Yield) of ethyl 7-methylimidazo[2,1-b]-benzthiazole-2-carboxylate was isolated as brown solid. (M+H) 261.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691842B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-480bbe16d45349ddabb275fd9489b7e4 |
| Source note | uspto-grants-2010_04 |