HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 135427949, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57503715 | HCID 57503715 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135427949 | HCID 135427949 | 83% |
Reaction Steps
10.5 ml (10.5 mmol) 1 M sodium hydroxide solution is added to 2.00 g (4.2 mmol) 3-(3-benzoylthioureido)-4-methyl-6-phenyl-thieno[2,3-b]-pyridine-2-carboxylic acid ethyl ester in 25 ml ethanol and refluxed for 30 min. Following the addition of 10 ml N,N-dimethylformamide, 5 ml (5 mmol) sodium hydroxide solution (1M) and 0.50 ml iodoethane (6.2 mmol) the next step is stirring at room temperature for 30 min. The precipitate precipitated following acidification with dilute hydrochloric acid is sucked off, washed with water, suck dried and dried in vacuo at 50° C. 1.23 g (83%) 2-ethylthio-9-methyl-7-phenyl-pyrido[3′,2′:4,5]thieno-[3,2-d]pyrimidin-4-one is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058285B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b91726d959404f9c9a8f009666ddecd8 |
| Source note | uspto-grants-2011_11 |