HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Cimetidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | CH2N2Pb | HCID 22262466 | — |
| Reactant | HCID 178486120 | HCID 178486120 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Cimetidine | HCID 178485005 | — |
Reaction Steps
Lead cyanamide (3.0 g.) was added to a solution of N-methyl-N'-[2-((4-methyl-5-imidazolyl)methylthio)-ethyl]thiourea (2.44 g.) in acetonitrile (50 ml.). Dimethylformamide (b 20 ml.) was added subsequently and the suspension was heated under reflux, with stirring, for 24 hours. Filtration, followed by concentration under reduced pressure and purification of the product by chromatography on a column of silica gel with acetonitrile as eluant and recrystallisation from the same solvent afforded N-cyano-N'-methyl-N"-[2-((4-methyl-5-imidazolyl)- methylthio)ethyl]guanidine, m.p. 139°-141°. (Found: C, 47.3; H, 6.6; N, 33.4; S, 12.6. C10N16N6S requires: C, 47.6; H, 6.4; N, 33.3; S, 12.7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04221802 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-82666c22d68e4f35aa3ad4bbfc77a705 |
| Source note | uspto-grants-1980_09 |