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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247713Generated: October 30, 2026

Carbon tetrabromide → Methyl 1-[(5-{5-[3-chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methyl]azetidine-3-carboxylate

https://huagongshe.com/reaction/2247713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl azetidine-3-carboxylate hydrochlorideHCID 21100040—
Reactant(5-{5-[3-Chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methanolHCID 68525419—
ProductMethyl 1-[(5-{5-[3-chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methyl]azetidine-3-carboxylateHCID 68523766—

Reaction Steps

The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 1 (1f) using (5-{5-[3-chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methanol (0.15 g, 0.34 mmol) that was obtained in Example 16 (16b), carbon tetrabromide (0.16 g, 0.51 mmol), triphenylphosphine (0.13 g, 0.51 mmol), methyl 3-azetidinecarboxylate hydrochloride (0.073 g, 0.51 mmol), and N,N-diisopropylethylamine (0.14 mL, 0.84 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (2:8 to 5:15) as the eluent to afford the title compound (0.16 g) in a yield of 88% as a colourless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-c8ab182a4d4a48bbadab4ec44f5650d1
Source noteuspto-grants-2010_03