HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-4-chloro-3-ethylisothiazole → HCID 22742112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-4-chloro-3-ethylisothiazole | HCID 9877468 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 2-[2-(2-methylpropyl)benzothiazol-5-yl]propionate | HCID 22742088 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 22742112 | HCID 22742112 | 65% |
Reaction Steps
5-Amino-4-chloro-3-ethylisothiazole (0.81 g, 0.005 mol) was added to a suspension of sodium methoxide (0.56 g, 0.010 mol) in tetrahydrofuran (5 ml) and the mixture stirred at room temperature for 25 minutes. A solution of methyl 2-[2-(2-methylpropyl)benzothiazol-5-yl]propionate (1.15 g, 0.004 mol) in tetrahydrofuran (4 ml) was added dropwise and the mixture stirred at room temperature for 1½ hours. The mixture was diluted with saturated aqueous ammonium chloride solution and extracted with dichloromethane. The organic extract was dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. Trituration with diethyl ether gave the desired product (1.06 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703347B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-6c19937bc9344f95a37626e2dfe904b9 |
| Source note | uspto-grants-2004_03 |