HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 5-(2-Cyano-1,1-dimethylethyl)-2-methylamino-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-(1-Chloro-2-methylpropan-2-yl)-N-methyl-1,3,4-thiadiazol-2-amine | HCID 12769656 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-(2-Cyano-1,1-dimethylethyl)-2-methylamino-1,3,4-thiadiazole | HCID 21430926 | — |
Reaction Steps
A 20.5 g. portion of the intermediate prepared in Example 1 and 10 g. of NaCN were added to 50 ml. of dimethylsulfoxide and heated at 110° C. for two hours. The reaction mixture was then cooled and poured into 300 ml. of water, which was then extracted with a total of 1 liter of ethyl ether. The combined ether extracts were dried over anhydrous Na2SO4, filtered, and evaporated to dryness yielding a dark oil. The oil was chromatographed on a silica gel column, eluting with ethyl acetate. The desired intermediate product, 5-(2-cyano-1,1-dimethylethyl)-2-methylamino-1,3,4-thiadiazole, m.p. 65°-67° C., was isolated in the amount of 750 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028090 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-d9f607598d5b4f118e071ff584f4083e |
| Source note | uspto-grants-1977_06 |