HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247729Generated: November 1, 2026
Carbon tetrabromide → HCID 68523928, compound
https://huagongshe.com/reaction/2247729
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl azetidine-3-carboxylate hydrochloride | HCID 21100040 | — |
| Reactant | HCID 68525865 | HCID 68525865 | — |
| Product | HCID 68523928 | HCID 68523928 | — |
Reaction Steps
The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 1 (1f) using (4-ethyl-5-{5-[3-fluoro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methanol (0.18 g, 0.43 mmol) that was obtained in Example 20 (20b), carbon tetrabromide (0.22 g, 0.65 mmol), triphenylphosphine (0.17 g, 0.65 mmol), methyl 3-azetidinecarboxylate hydrochloride (99 mg, 0.65 mmol), N,N-diisopropylethylamine (0.22 mL, 1.3 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 (1:3 to 1:2) as the eluent to afford the title compound (0.14 g) in a yield of 64% as a pale yellow 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-cf7567cde00e47808d091e9db062aea7 |
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| Source note | uspto-grants-2010_03 |
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