HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76994Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 46840710, compound
https://huagongshe.com/reaction/76994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-Quinuclidinol, (-)- | HCID 91404 | — |
| Reactant | (2-Ethyl-phenylamino)-phenyl-acetic acid hydrochloride | HCID 67424496 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46840710 | HCID 46840710 | 21% |
Reaction Steps
PS-DCC (962 mg, 1.37 mmol, loading: 1.33 mmol/g) is suspended in THF (10 mL). HOBT (210 mg, 1.37 mmol), (2-ethyl-phenylamino)-phenyl-acetic acid hydrochloride (160) (200 mg, 0.68 mmol), and (R)-quinuclidin-3-ol (262 mg, 2.06 mmol) are added and the mixture is shaken at RT overnight. PS-DCC is filtered off and washed with THF and the filtrate is evaporated under reduced pressure. The resulting residue is dissolved in EtOAc and washed with sat. NaHCO3, water and brine. The organic layer is separated, dried over Na2SO4, filtered and evaporated. The residue is first purified by flash chromatography (DCM/MeOH=9/1) and then by preparative HPLC. The fractions containing the product are pooled, concentrated under vacuum, basified with sat. NaHCO3 and extracted with EtOAc. The organic layer is dried (Na2SO4), filtered and evaporated to afford the title compound as a colorless oil (52 mg, 21% yield, mixture of diastereoisomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08835682B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-17f385bb58c34ee4988f82c00b527154 |
|---|
| Source note | uspto-grants-2014_09 |
|---|