HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273784Generated: October 31, 2026
Dimethylformamide → HCID 135715021, compound
https://huagongshe.com/reaction/273784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20093979 | HCID 20093979 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 135715021 | HCID 135715021 | — |
Reaction Steps
5. 15.2 g of 5-(chloromethyl)thieno[2,3-e][1,2,4]triazolo[4,3-c]pyrimidine are suspended in 650 ml of dioxan and 43 ml of dimethylformamide and cooled to 5° C. 86 ml of 1N sodium hydroxide solution are added thereto within 3 min. and the mixture is stirred at room temperature for 17 h. The reaction mixture is then partitioned between 1.5 l of saturated aqueous sodium chloride solution and 0.7 l of chloroform. The aqueous phase is then made weakly acidic (pH 6) with 12N hydrochloric acid. The mixture is extracted five times with chloroform. The organic extracts are concentrated in a vacuum. The crystalline residue is recrystallized from ethanol. There is obtained 5H-thieno[2,3-f][1,2,4]triazolo[1,5-d][1,4]diazepin-6(7H)-one of m.p. 213°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05387585 |
|---|
| Source dataset | uspto-grants-1995_02 |
|---|
| ORD ID | ord-c4aef13f595e4521920499970005ecda |
|---|
| Source note | uspto-grants-1995_02 |
|---|