HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247647Generated: October 30, 2026
Carbon tetrabromide → HCID 68526579, compound
https://huagongshe.com/reaction/2247647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl azetidine-3-carboxylate hydrochloride | HCID 44828820 | — |
| Reactant | HCID 68521108 | HCID 68521108 | — |
| Product | HCID 68526579 | HCID 68526579 | — |
Reaction Steps
The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 1 (1f) using (4-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methanol (0.10 g, 0.25 mmol) that was obtained in Example 3 (3c), carbon tetrabromide (0.17 g, 0.50 mmol), triphenylphosphine (0.13 g, 0.50 mmol), ethyl 3-azetidinecarboxylate hydrochloride (62 mg, 0.38 mmol), and N,N-diisopropylethylamine (0.11 ml, 0.63 mmol). Subsequently, the crude product of the title compound thus obtained was purified by thin layer chromatography on a silica gel plate using a mixed solvent of ethyl acetate and hexane (2:3) as the developing solvent to afford the title compound (73 mg) in a yield of 56% as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07687491B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-747193c568c743ef9737f2b2f68dd068 |
|---|
| Source note | uspto-grants-2010_03 |
|---|