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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250284Generated: November 2, 2026

1,1'-(Azodicarbonyl)dipiperidine → 5-(4-(5-Cyclopropyl-3-(2,6-dichloro-phenyl)-isoxazol-4-ylmethoxy)-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/250284

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant(5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanolHCID 45790382—
Reactant5-(4-Hydroxy-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl esterHCID 57443286—
SolventTolueneHCID 1140—
Product5-(4-(5-Cyclopropyl-3-(2,6-dichloro-phenyl)-isoxazol-4-ylmethoxy)-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl esterHCID 5808835645.4%

Reaction Steps

To a solution of (5-cyclopropyl-3-(2,6-dichloro-phenyl)-isoxazol-4-yl)-methanol (0.188 g, 0.66 mmol), 5-(4-hydroxy-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl ester (0.15 g, 0.60 mmol), and tri-N-butyl-phosphine (0.16 g, 0.79 mmol) in toluene (2 mL) is added a solution of ADDP (0.2 g, 0.79 mmol) in 1 mL of toluene. The reaction is stirred overnight. The reaction mixture is partitioned between ethyl acetate and water and the layers are separated. The organic layer is washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield a crude oil. The oil is chromatographed using a gradient of 10% ethyl acetate in hexanes to 40% ethyl acetate in hexanes to yield the title compound (0.14 g, 41%). ES/MS m/e 514.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863302B2
Source datasetuspto-grants-2011_01
ORD IDord-11ec63371a9043fba1638f1c68e218c1
Source noteuspto-grants-2011_01