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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | (5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol | HCID 45790382 | — |
| Reactant | 5-(4-Hydroxy-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl ester | HCID 57443286 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(4-(5-Cyclopropyl-3-(2,6-dichloro-phenyl)-isoxazol-4-ylmethoxy)-2-methyl-phenyl)-thiophene-2-carboxylic acid methyl ester | HCID 58088356 | 45.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863302B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-11ec63371a9043fba1638f1c68e218c1 |
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| Source note | uspto-grants-2011_01 |
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