HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-(2-Ethoxycarbonyl-benzo[b]thiophen-6-yloxy)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | Ethyl 6-hydroxybenzo[b]thiophene-2-carboxylate | HCID 58047243 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Ethoxycarbonyl-benzo[b]thiophen-6-yloxy)-piperidine-1-carboxylic acid tert-butyl ester | HCID 68726581 | 94.4% |
Reaction Steps
The above prepared 6-hydroxy-benzo[b]thiophene-2-carboxylic acid ethyl ester (0.206 g, 0.927 mmol, see example 7, step 1 and 2) was dissolved in 5 mL of THF and treated successively at −10° C. with 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (0.261 g, 1.4 eq.), triphenylphosphine (0.340 g, 1.4 eq.) and DIAD (0.255 mL, 2 eq.), and the mixture then kept at ambient temperature over night. Pouring onto crashed ice, twofold extraction with AcOEt, washing with water and brine, drying over magnesium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, hexane AcOEt=85/15), yielded 0.355 g of the title compound as colorless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534788B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f4fc7e9fcad54b32879d46e56b223619 |
| Source note | uspto-grants-2009_05 |