HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 20435920, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-[(2-Bromoethyl)sulfanyl]ethan-1-one | HCID 523036 | — |
| Reactant | HCID 13774859 | HCID 13774859 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20435920 | HCID 20435920 | 7% |
Reaction Steps
(c) A solution of 1.27 g of tert.butyl hexahydro-1,3-dioxo-1H-pyrazolo[1,2-a]pyridazine-5-carboxyate in 10 ml of dimethylformamide was added to a suspension of 0.4 g of sodium hydride in dimethyformamide. The mixture was stirred at room temperature until the evolution of gas had ceased. 1.86 g of S-bromoethyl thioacetate were added and the mixture was heated at 75° C. for 5 hours. Working-up in the same manner as described in paragraph (D) (a) earlier gave 0.15 g (7%) of tert.butyl 2,2- bis(acetylthiomethyl)-hexahydro-1,3-dioxo-1H-pyrazolo[1,2-a]pyridazine-5-carboxylate in the form of a white solid having a melting point of 85°-86° C. (from diethyl ether/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04487929 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-325f293f7cd84853b798823869deef6a |
| Source note | uspto-grants-1984_12 |