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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975682Generated: October 25, 2026

2-Furanmethanethiol → 8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide

https://huagongshe.com/reaction/1975682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FuranmethanethiolHCID 7363—
ReactantPiperidineHCID 8082—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantHCID 10831197HCID 10831197—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10742479—

Reaction Steps

A solution of 8-chloro-N-(2-oxo-3-butenyl)dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide (0.75 gram), furfuryl mercaptan (0.23 mL), piperidine (0.069 mL), and N-benzyltrimethylammonium hydroxide (0.069 mL) in methylene chloride (12 mL) and methanol (3 mL) was stirred at room temperature for 6 hours. The reaction was diluted with methylene chloride (75 mL), washed with 75 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (350 mL) using 95:5 methylene chloride: ethyl acetate to yield a colorless oil. Analysis calculated for C23H21ClN2O4S×0.1 EtOAc: C, 60.34; H, 4.72; N, 6.01; Cl, 7.61; S, 6.88. Found: C, 59.94; H, 4.84; N, 5.87; Cl, 8.13; S, 6.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288719
Source datasetuspto-grants-1994_02
ORD IDord-656a33c26a63406d8f84e3a23f931ab8
Source noteuspto-grants-1994_02