HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 9957047, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 14071251 | HCID 14071251 | — |
| Reactant | HCID 178447642 | HCID 178447642 | — |
| Product | HCID 9957047 | HCID 9957047 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Into a one liter reactor fitted with stirring, cooling and warming means and placed under nitrogen circulation were poured 30 ml of dimethylformamide, 20.3 g (0.055 mol) of 6-(2-chlorophenyl)-7, 8, 9, 10 -tetrahydro-1-methyl-4H-pyrido [4',3':4,5] thieno [3,2-f] 1,2,4-triazolo [4,3-a] 1,4-diazepine and 8.9 g (0.058 mol) of isopropyl-thio-acetic acid. After cooling the mixture to 0° C., there were slowly added, under stirring, 12.36 g (0.058 mol) of dicyclohexylcarbodiimide. Stirring was maintained for 4 hours at 0° C. and then for one hour after the reaction mixture had reached room temperature. There were then added 2 g of dicyclohexylcarbodiimide and the mixture was stirred overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05049559 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-5bda237e662d4d3eaa1c7742a839b932 |
| Source note | uspto-grants-1991_09 |