Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929530Generated: November 1, 2026

Sodium hydride → HCID 86632299, compound

https://huagongshe.com/reaction/1929530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Cyano-4-fluorobenzylcyanideHCID 2773936—
Reactant3,6-Dichloro-4-isopropylpyridazineHCID 14024162—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86632299HCID 86632299—

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice-cold solution of 5-(cyanomethyl)-2-fluorobenzonitrile (1 eq) and 3,6-dichloro-4-isopropylpyridazine (1.3 eq) (Reference: Org. Prep.+Proc. Int. 1988, 20, 117 and U.S. Pat. No. 4,628,088, 1986) in THF (38 mL, 0.1 M) was added portionwise NaH (1 eq). The reaction was stirred at 0° C. for 15 min and then warmed to RT and stirred for 2 hrs. The reaction was quenched with a sat. aq. NaHCO3 and extracted with EtOAc. The combined organic fractions were washed with brine, dried (Na2SO4) and concentrated under reduced pressure. The crude was purified by silica gel chromatography, eluting with petroleum ether:EtOAc (8:2) to afford the title compound. 1H NMR (400 MHz, CDCl3) δ: 7.80-7.79 (2H, m), 7.49 (1H, s), 7.31-7.29 (1H, m), 5.63 (1H, s), 3.34-3.28 (1H, m), 1.36-1.29 (6H, m). MS (ES) C16H12ClFN4 required: 314/316. found: 315/317 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188084B2
Source datasetuspto-grants-2012_05
ORD IDord-4676f021764847a682c5cf1f61d86b89
Source noteuspto-grants-2012_05