HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 53870194, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-(2-Aminoethylthiomethyl)-6-(dimethylaminomethyl)benzofuran | HCID 20303964 | — |
| Reactant | Methanesulfonyliminodithiocarbonic acid dimethyl ester | HCID 86734341 | — |
| Product | HCID 53870194 | HCID 53870194 | — |
Reaction Steps
A solution of 2-(2-aminoethylthiomethyl)-6-(dimethylaminomethyl)benzofuran (Example 1, Step E) (2.6 g., 0.01 mole) and methanesulfonyliminodithiocarbonic acid dimethyl ester (2.0 g., 0.01 mole) in methanol (15 ml.) is kept at 25°-27° C. for 4 hours. A solution of 10 g. of methylamine in 35 ml. of methanol is added and the resulting solution is kept at 25°-27° C. for 16 hours. The solvent is evaporated to leave N-[2-(6-dimethylaminomethyl-2-benzofuranylmethylthio)-ethyl]-N'-methanesulfonyl-N"-methylguanidine as a residual oil which is purified by column chromatography (silica gel/5% methanol in chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238487 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-7c79e4963c6a4b95b6cbf5f27f08ab09 |
| Source note | uspto-grants-1980_12 |