HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 66874427, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-chlorobenzo[d]oxazole-4-carboxylate | HCID 56924368 | — |
| Reactant | HCID 66874002 | HCID 66874002 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 66874427 | HCID 66874427 | 43% |
Reaction Steps
To a solution of (S)-1-allyl-3-isobutylpiperazine (442 mg, 2.42 mmol) in DME (10 mL) at room temperature, was added NaH (60% suspension in mineral oil, 100 mg, 2.42 mmol) and the mixture was stirred for 45 min. Methyl 2-chlorobenzoxazole-4-carboxylate (510 mg, 2.42 mmol) was added to the reaction mixture and the reaction was stirred at room temperature for 17 h. The reaction mixture was quenched with CH3OH (10 mL), silica gel (15 mL) was added, and solvent removed under reduced pressure. The mixture was purified by column chromatography (silica gel, 10:1:0.1 CH2Cl2/CH3OH/concentrated NH4OH) to afford methyl 2-(4-allyl-(S)-2-isobutylpiperazine-1-yl)benzoxazole-4-carboxylate (372 mg, 43%) as a yellow oil. 1H NMR and MS consistent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863271B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-20527bbd118546aa9a668bfd3ef30dc9 |
| Source note | uspto-grants-2011_01 |