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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759252Generated: November 1, 2026

Diethyl Ether → HCID 70543458, compound

https://huagongshe.com/reaction/1759252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantPhenylsulphonyl isocyanateHCID 76096—
ReactantHCID 70543093HCID 70543093—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70543458HCID 7054345826.2%

Reaction Steps

Phenyl sulphonyl isocyanate (1.2 g) was added to a suspension of 3-(4-carboxybenzyloxy) 2-(1-imidazolylmethyl)pyridine (1.0 g) in dry tetrahydrofuran (40 ml) containing triethylamine (0.33 g). The mixture was stirred at room temperature for 8 hours and allowed to stand at room temperature for a further 36 hours. The solvents were evaporated under vacuum and aqueous 5% sodium bicarbonate solution (100 ml) added to the residue. The mixture was extracted with dichloromethane (3×50 ml) and the combined organic extracts dried, filtered and evaporated to yield an oil which solidified on trituration with diethyl ether. Recrystallization from aqueous methanol gave 2-(1-imidazolylmethyl)-3-[4-(N-phenylsulphonylcarbamoyl)benzyloxy]pyridine (0.38 g), m.p. above 250° C. Found: C, 61.47; H, 4.40; N, 12.63. C23H20N4O4S requires: C, 61.59; H, 4.50; N, 12.49%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04339583
Source datasetuspto-grants-1982_07
ORD IDord-a3b09942bcdb4c10a860a102600a8e7a
Source noteuspto-grants-1982_07