HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-Methyl-thiophene-2-carboxylic acid (4-chloro-benzothiazol-2-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Benzothiazolamine, 4-chloro- | HCID 29872 | — |
| Reactant | 5-Methylthiophene-2-carbonyl chloride | HCID 2760083 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Methyl-thiophene-2-carboxylic acid (4-chloro-benzothiazol-2-yl)-amide | HCID 86584916 | — |
Reaction Steps
2-Amino-4-chlorobenzothiazol (92 mg, 0.50 mmol) is dissolved in dichloromethane (10 ml) and treated with pyridine (0.060 ml, 0.75 mmol) and 5-methyl-thiophene-2-carbonyl chloride (97 mg, 0.60 mmol). The reaction mixture is stirred at ambient temperature for 18 h and then evaporated to dryness. The residue is redissolved in ethyl acetate and water, the phases are separated and the organic layer extracted with brine. After dryin with sodium silfate, the solvent is removed in vacuo Flash chromatography on silica (eluent ethyl acetate/cyclohexane 1:4 affords the product as white solid.(88 mg, 57%). MS: m/e=308 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06963000B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-3f6db65703314a8cac3e708e206d598a |
| Source note | uspto-grants-2005_11 |