Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058567Generated: November 1, 2026

Isoamyl Nitrite → HCID 18668822, compound

https://huagongshe.com/reaction/1058567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 18668835HCID 18668835—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 18668822HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518266B1
Source datasetuspto-grants-2003_02
ORD IDord-fcf26098e7664bafbfe653932d3fb040
Source noteuspto-grants-2003_02