HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 5-Methyl-thiophene-2-carboxylic acid (4-methoxy-7-piperazin-1-yl-benzothiazol-2-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 4-{4-Methoxy-2-[(5-methyl-thiophene-2-carbonyl)-amino]-benzothiazol-7-yl}-piperazine-1-carboxylic acid benzyl ester | HCID 86584912 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Methyl-thiophene-2-carboxylic acid (4-methoxy-7-piperazin-1-yl-benzothiazol-2-yl)-amide | HCID 86584942 | 58% |
Reaction Steps
To a solution of 4-{4-methoxy-2-[(5-methyl-thiophene-2-carbonyl)-amino]-benzothiazol-7-yl}-piperazine-1-carboxylic acid benzyl ester (300 mg, 0.57 mmol) in dichloromethane (5 ml) were added boron trifluoride diethyl etherate (0.72 ml, 5.7 mmol) and ethane thiol (1.2 ml, 17 mmol) and the mixture stirred for 36 h. The volatile components are evaporated and the residue codistilled twice with toluene. The residue was dissolved in dichloromethane (25 ml), extracted with 1N aqueous sodium carbonate and the organic phase dryed with Na2SO4. Removal of the solvent and flash chromatography (silica, eluent CH2Cl2/MeOH/aqu. NH4OH 100:10:1) afforded the title compound as light yellow solid (58%), MS: m/e=389 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317007B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-67f7a3e316754c788d47a3dcb9878915 |
| Source note | uspto-grants-2008_01 |