HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → HCID 54199411, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 178503919 | HCID 178503919 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54199411 | HCID 54199411 | — |
Reaction Steps
Methyl hydrazine (6.9 g) and dry dimethylformamide (10.95 g) were heated at reflux in toluene for 1 hr. N'-Cyano-N-[3-[3-(1-pyrrolidinylmethyl)phenoxy]propyl]carbamimidothioic acid, methyl ester (10 g) was then adde and the mixture heated at reflux for 5 hr. Evaporation of the solvent gave the title compound as a yellow oil which was converted to the fumarate salt in ethanol. The title compound was regenerated as the free base with aqueous sodium carbonate, and extracted into ethyl acetate. Evaporation of the solvent and trituration of the residue with light petroleum (b.p. 60°-80°) gave the title compound as a white solid (3.4 g) m.p. 95°-95.5°. TLC silica; methanol:0.88 ammonia (80:1) single spot Rf 0.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764612 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-be0e956cb0ac4935bdca9d449076a46a |
| Source note | uspto-grants-1988_08 |