Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355580Generated: November 1, 2026

Diisopropyl Ether → HCID 178451562, compound

https://huagongshe.com/reaction/1355580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178479294HCID 178479294—
SolventIsopropanolHCID 3776—
ProductHCID 178451562HCID 17845156279.8%

Reaction Steps

To a solution of (1R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-imidazol-2-yl)-1-ethanamine hydrochloride (14 g, 35 mmol) in isopropanol (210 ml) was added 1-tert-butoxycarbonyl-4-piperidone (35 g, 170 mmol) and the mixture refluxed for about two hours. The solvent was evaporated under reduced pressure. Water (150 ml) was added to the residue followed by 10% NaHCO3 solution until neutral pH and extracted by ethyl acetate (4×50 ml). The combined organic extracts were washed with water (2×50 ml) and dried over MgSO4. The solvent was removed under reduced pressure to afford an oil which solidified on addition of diisopropyl ether (150 ml). The precipitate was collected by filtration, washed with diisopropyl ether and dried to afford 13.5 g of the desired product. Melting point: 118-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586445B1
Source datasetuspto-grants-2003_07
ORD IDord-571d1c2b625e479fbdac98b516dd6b76
Source noteuspto-grants-2003_07