HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 19349406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | S-methyl isothiourea hemisulfate | HCID 6604939 | — |
| Reactant | HCID 19349446 | HCID 19349446 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19349406 | HCID 19349406 | — |
Reaction Steps
A mixture of the product from Example 28 (0.6 g), S-methylthiouronium sulphate (0.56 g), 10N aqueous sodium hydroxide (1 ml) and dimethylformamide (5 ml) was stirred at room temperature for 18 h, diluted with water (20 ml) and extracted twice with dichloromethane. The extracts were combined, dried and evaporated to dryness under reduced pressure, and the residue was purified by flash column chromatography, eluting with methanol:ethyl acetate (1:49 by volume) to give 2-methyl-2-[3-methylthiomethyl-5-(1H-1,2,4-triazol-1-ylmethyl)phenyl]-propiononitrile. Nmr in deuteriochloroform: δ 8.12(1H,s), 8.0(1H,s), 7.4(1H,m), 7.27(1H,m), 7.15(1H,m), 5.38(2H,s), 3.66(2H,s), 2.0(3H,s), 1.72(6H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935437 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-2e838140041a4217a6b83fe8aece84d4 |
| Source note | uspto-grants-1990_06 |