HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(dimethoxymethyl)-N-methylethanamine → N'-(4-{[3-(3-Chlorobenzyl)-1,2,4-thiadiazol-5-yl]oxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(dimethoxymethyl)-N-methylethanamine | HCID 23017846 | — |
| Reactant | HCID 67080809 | HCID 67080809 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N'-(4-{[3-(3-Chlorobenzyl)-1,2,4-thiadiazol-5-yl]oxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide | HCID 44546592 | 27.6% |
Reaction Steps
1.85 g (5.15 mmol) of 4-{[3-(3-chlorobenzyl)-1,2,4-thiadiazol-5-yl]oxy}-2,5-dimethylaniline are dissolved in 10 ml of toluene and treated with 1.37 g (10.31 mmol) of N-ethyl-N-methylformamide dimethylacetal. The reaction mixture is refluxed for 12 h, subsequently cooled, freed of solvent under vacuum and purified by column chromatography. 0.59 g of product is obtained (99.0% purity, 27.3% yield; log P (pH2.3)=2.31).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383139B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-488bfa76755140808b27e2978315145d |
| Source note | uspto-grants-2013_02 |