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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991492Generated: November 2, 2026

Ammonium Chloride → HCID 178432683, compound

https://huagongshe.com/reaction/991492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
ReactantN,2-Dimethyl-3-pyridinecarboxamideHCID 12833322—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 178432683HCID 178432683—

Reaction Steps

To a solution of 4-iodo-1-tritylimidazole (6.88 g, 15.8 mmol) in 65 mL anhydrous dichloromethane was added 6.3 mL of a solution of ethyl magnesium bromide (3.0 M, 18.9 mmol) in diethyl ether under argon. The reaction mixture was stirred for 2.5 h, and then a solution of N-methoxy, N-methyl-2-methylnicotinamide (2.84 g, 15.8 mmol) was added. After 5 days of stirring, the reaction mixture was poured into saturated aqueous ammonium chloride solution (125 mL). The layers were separated, and the aqueous layer was extracted twice with dichloromethane (50 mL). The organic extracts were combined, dried (Na2SO4), and concentrated to provide a red-orange foam which was purified on flash silica gel (1% methanol-chloroform to 2% methanol-chloroform) to provide the desired product as 5.56 g (82%) of a golden-brown foam. MS (PB-NH3), m/z 430 (MH+). 1H NMR (CDCl3) δ 2.63 (s, 3H), 7.02-7.16 (m, 7H), 7.19 (dd, J=7.8, 5.1 Hz, 1H), 7.28-7.41 (m, 8H), 7.49 (d, J=0.9 Hz, 1H), 7.70 (d, J=0.9 Hz, 1H), 7.96 (dd, J=7.9, 1.2 Hz, 1H), 8.57 (dd, J=7.9, 4.9 Hz, 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465486B1
Source datasetuspto-grants-2002_10
ORD IDord-731ae8ac3bcb48a9b540a308ec397f93
Source noteuspto-grants-2002_10