HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 14998282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methoxy-N-methylcarbamoyl chloride | HCID 2734926 | — |
| Reactant | HCID 14998281 | HCID 14998281 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14998282 | HCID 14998282 | 73.1% |
Reaction Steps
2.2 g of 2-[2-(2,3-dihydro-2,2-dimethyl-5-benzofuranyl)ethoxy]-5-aminopyridine was dissolved into 10 ml of N,N-dimethylformamide, and 0.9 g of triethylamine was added thereto. 1.2 g of N-methoxy-N-methylcarbamoyl chloride was slowly added dropwise thereto. After the mixture was stirred at room temperature, the reaction mixture was poured into water and extracted with ethyl acetate. After the organic layer was washed with water, it was dried over anhydrous magnesium sulfate and ethyl acetate was dried off. The residue was subjected to silica gel column chromatography using ethyl acetate/n-hexane (2/3) as a developer to obtain 2.1 g of 1-{2-[2-(2,3-dihydro-2,2-dimethyl-5-benzofuranyl)ethyloxy]-5-pyridyl}-3-methoxy-3-methylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959092 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-4b58a5b6d8c44fc7813a1ef5915854c7 |
| Source note | uspto-grants-1990_09 |