HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoamyl Nitrite → HCID 18668822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | HCID 18668835 | HCID 18668835 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18668822 | HCID 18668822 | — |
Reaction Steps
A solution of aminopyrazole 41 (42 mg, 0.1 mmol) in DMF (5 mL) was warmed up to 65° C. and treated dropwise with excess isoamyl nitrite (150 mL). Stirring was continued for 30 min. The reaction was cooled down to room temperature, diluted with ethyl ether (10 mL) and washed with brine (5×15 mL). The organic layer was dried (magnesium sulfate) and the solvents removed at reduced pressure, leaving a dark oil residue. The desired product was obtained upon flash chromatography eluting with ethyl acetate-hexanes (5-10%), to yield 14 mg (35%) of desired product. 1H-NMR (δ, CDCl3): 2.63 (3H, s); 7.78 (2H, s); 8.1 (1H, s); 8.28 (1H, d, J=2.5 Hz); 8.4 (1H, dd, J=1.4; 8.4 Hz); 9.2 (1H, d, J=1.5 Hz). MS: M+1=404 (calculated: 404).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518266B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-fcf26098e7664bafbfe653932d3fb040 |
| Source note | uspto-grants-2003_02 |