HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Methoxy-N-(4-methoxy-7-phenyl-benzothiazol-2-yl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methoxybenzoyl chloride | HCID 88969 | — |
| Reactant | 2-Amino-4-methoxy-7-phenyl-benzothiazole | HCID 22283026 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-N-(4-methoxy-7-phenyl-benzothiazol-2-yl)-benzamide | HCID 22283400 | — |
Reaction Steps
To a solution of 2-amino-4-methoxy-7-phenyl-benzothiazole (200 mg, 0.67 mmol) in THF (10 m) was added DMAP (10 mg, 0.08 mmol), triethylamine (163 □l, 1.17 mmol) and 2-methoxybenzoyl chloride (136 □1, 1 mmol) in THF (2 ml). The mixture was then heated to reflux for 2 h, after cooling, it was partitioned between 1:1 AcOEt/THF (70 ml) and 5% NaHCO3 solution( 40 ml). The organic phase was washed with saturated NaCl solution (50 ml), dried with Na2SO4, filtered and the solvent removed under reduced presure. The residue was suspended in ether (10 ml), filtered, washed with ether then dried under vacuum (0.05 mmHg, 60 ° C.), to afford the title compound was a white solid (260 mg, 85% yield), MS: m/e=390.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06521754B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-2c2704a95ed34c91a9a2d462706022cb |
| Source note | uspto-grants-2003_02 |