HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 54553130, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-DICHLOROPYRIDO[3,2-D]PYRIMIDINE | HCID 11958053 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54553130 | HCID 54553130 | 65% |
Reaction Steps
A suspension of 15 gm (0.075 mol) of 2,4-dichloropyrido[3,2-d]pyrimidine in 100 ml of acetone at -40°C was admixed with a solution of 3.2 gm (0.08 mol) of sodium hydroxide and 4.9 gm (5.8 ml) of ethylmercaptan in 25 ml of water, and the mixture was stirred for two hours at room temperature. Thereafter, 200 ml of water were added to the reaction mixture, and the precipitate formed thereby was collected and recrystallized from petroleum ether, yielding 11.0 gm (65% of theory) of 2-chloro-4-ethylmercapto-pyrido[3,2-d]pyrimidine, m.p. 101°-103°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03939268 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-a75d9329604c4255b2c6c06a9e159a1c |
| Source note | uspto-grants-1976_02 |