HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → N-(3-azidopropyl)-4,6-dichloro-1,3,5-triazin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Azidopropan-1-amine | HCID 150110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(3-azidopropyl)-4,6-dichloro-1,3,5-triazin-2-amine | HCID 86672179 | 45.3% |
Reaction Steps
To a solution of cyanuric chloride (18.42 g, 0.10 mol) in acetone (180 mL) in an ice-water bath was added diisopropylethylamine (DIPEA) (12.92 g, 0.10 mol). 1-azido-3-aminopropane (5.00 g, 0.050 mol) in acetone (50 mL) was added slowly over 2 hours. The reaction was stirred at room temperature overnight. The solvent was removed under reduced pressure. The residue was dissolved in CH2Cl2, washed with water, dried (Na2SO4) and rotary evaporated. The resulting residue was purified by column chromatography on silica gel (eluent CH2Cl2) to give 1 as a white solid (5.62 g, 45%): ESI-MS m/z 248.1 (M+H+) calculated for C6H8Cl2N7 248.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912323B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-9b9522b2d31340ccb5a87aa75cc45e6f |
| Source note | uspto-grants-2014_12 |