HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 6-[[4-[3-(Trifluoromethyl)-phenoxy]butyl]thio]-3-pyridazinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Chlorobutoxy)-3-(trifluoromethyl)-benzene | HCID 12928641 | — |
| Reactant | HCID 178514135 | HCID 178514135 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-[[4-[3-(Trifluoromethyl)-phenoxy]butyl]thio]-3-pyridazinecarbothioamide | HCID 18176642 | 47.1% |
Reaction Steps
A mixture of intermediate 11 (0.017 mol) in DMF (80 ml) was stirred at room temperature. Sodium hydride (50%, 0.02 mol) was added portionwise. The mixture was stirred for 30 minutes. A mixture of 1-(4-chlorobutoxy)-3-(trifluoromethyl)-benzene (0.02 mol) in DMF (20 ml) was added dropwise. The mixture was stirred at room temperature overnight. The solvent was evaporated. The residue was stirred in DIPE (100 ml), filtered off and dried, yielding 3.1 g (47%) of 6-[[4-[3-(trifluoromethyl)-phenoxy]butyl]thio]-3-pyridazinecarbothioamide (intermediate 12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06602873B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-8da87fa6bb7c48b6a499ea97f4c6e60d |
| Source note | uspto-grants-2003_08 |