HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → HCID 136113976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 136029103 | HCID 136029103 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 136113976 | HCID 136113976 | 143.1% |
Reaction Steps
A suspension of 8.9 g of 5-(2-chlorophenyl)-7-[4-(4-isobutylphenyl)butyl]-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one, melting at 133°-135° C. and 4.7 g of Lawesson reagent in 100 ml of toluene is stirred at 38°-40° C. for an hour. The resultant solution is concentrated under reduced pressure, and the residue is subjected to chromatography on silica gel and then eluted with chloroform-methanol (100:1 to 100:2). The objective fraction is concentrated under reduced pressure to give 8 g of 5-(2-chlorophenyl)-7-[4-(4-isobutylphenyl)butyl]-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepine-2-thione, melting at 169°-171° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04820703 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-c21fdb86173541808b1fde7abdfdd813 |
| Source note | uspto-grants-1989_04 |