HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-[[(7-chloro-2,2,3,3-tetrafluorobenzothien-5-yl)amino]-carbonyl]-2-chlorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Chlorobenzamide | HCID 69111 | — |
| Reactant | 5-Amino-7-chloro-2,2,3,3-tetrafluoro-2,3-dihydrobenzothiophene | HCID 20222418 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[[(7-chloro-2,2,3,3-tetrafluorobenzothien-5-yl)amino]-carbonyl]-2-chlorobenzamide | HCID 13785000 | 51.7% |
Reaction Steps
In a manner similar to Step D of Example 1, the reaction of 0.58 g (0.0037 mole) 2-chlorobenzamide, 0.52 g (0.0051 mole) oxalyl chloride, 0.95 g (0.0037 mole) 5-amino-7-chloro-2,2,3,3-tetrafluoro-2,3-dihydrobenzothiophene, and 5 ml of methylene chloride in 75 ml of toluene produced 0.84 g of N-[[(7-chloro-2,2,3,3-tetrafluorobenzothien-5-yl)amino]-carbonyl]-2-chlorobenzamide as a solid (mp 140°-142° C.), compound 9 of Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636523 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-478995f7001b4f6da4bccc09efe97d9c |
| Source note | uspto-grants-1987_01 |