HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Diethyl-1,3-propanediamine → 1-(4-Chloropyridin-2-yl)-3-(3-diethylaminopropyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Diethyl-1,3-propanediamine | HCID 61011 | — |
| Reactant | Phenyl (4-chloropyridin-2-yl)-N-(phenoxycarbonyl)carbamate | HCID 21054897 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Chloropyridin-2-yl)-3-(3-diethylaminopropyl)urea | HCID 21949093 | 54.5% |
Reaction Steps
Phenyl(4-chloropyridin-2-yl)-N-(phenoxycarbonyl)carbamate (738 mg, 2.00 mmol) was dissolved in N,N-dimethylformamide (8.0 ml); N,N-diethyl-1,3-diaminopropane (1.57 ml, 10.0 mmol) was added thereto; and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was partitioned between water and ethyl acetate; and the organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, hexane-ethyl acetate-methanol system) to yield the title compound (309 mg, 1.09 mmol, 54.3%) as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109219B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-b2d57b0db43d419c90334ae4babe0c6f |
| Source note | uspto-grants-2006_09 |