HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247762Generated: October 26, 2026
Carbon tetrabromide → Methyl 1-({5-[5-(3-chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]-6-ethylpyridin-2-yl}methyl)azetidine-3-carboxylate
https://huagongshe.com/reaction/2247762
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl azetidine-3-carboxylate hydrochloride | HCID 21100040 | — |
| Reactant | {5-[5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]-6-ethylpyridin-2-yl}methanol | HCID 68521068 | — |
| Product | Methyl 1-({5-[5-(3-chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]-6-ethylpyridin-2-yl}methyl)azetidine-3-carboxylate | HCID 68524350 | — |
Reaction Steps
The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 23 (23g) using {5-[5-(3-chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]-6-ethylpyridin-2-yl}methanol (0.15 g, 0.40 mmol) that was obtained in Example 25 (25c), carbon tetrabromide (0.27 g, 0.80 mmol), triphenylphosphine (0.21 g, 0.80 mmol), methyl 3-azetidinecarboxylate hydrochloride (91 mg, 0.60 mmol) and N,N-diisopropylethylamine (0.21 ml, 1.2 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 (1:1 to 2:1 or 3:1) as the eluent to afford the title compound (0.16 g) in a yield of 83% as a pale yellowish oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687491B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-15bf9bb01f144fc2895ef014ce3b973a |
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| Source note | uspto-grants-2010_03 |
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