Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 559324Erstellt: 26. Oktober 2026

Acetic Acid → 4-[3-((R)-2-Hydroxymethyl-pyrrolidin-1-yl)-propyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/559324

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAmmonium HydroxideHCID 14923—
EduktBorane;pyridineHCID 2723995—
EduktProlinol, (R)-HCID 2724541—
EduktSodium periodateHCID 23667635—
EduktTert-butyl 4-but-3-enyl-3-oxopiperazine-1-carboxylateHCID 57445033—
KatalysatorOsmium TetroxideHCID 30318—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelEthanolHCID 702—
LösungsmittelPropan-2-one--water (1/1)HCID 18366337—
Produkt4-[3-((R)-2-Hydroxymethyl-pyrrolidin-1-yl)-propyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl esterHCID 6699954060%

Reaktionsschritte

Sodium metaperiodate (505 mg, 2.36 mmol) and osmium(VIII) oxide (2.5% solution in tert-butylalcohol, 80 μl, 7.9 μmol) were added at 0° C. to a solution of 4-but-3-enyl-3-oxo-piperazine-1-carboxylic acid tert-butyl ester (200 mg, 0.79 mmol) in acetone/water 1:1 (10 ml). After 30 min, the reaction mixture was allowed to reach room temperature over 45 min, then partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (MgSO4), and evaporated. The crude aldehyde intermediate (3-oxo-4-(3-oxo-propyl)-piperazine-1-carboxylic acid tert-butyl ester) and D-prolinol (95 mg, 0.94 mmol) were dissolved in 1,2-dichloroethane (2 ml), then a freshly prepared solution of pyridine borane complex (8 M in pyridine, 0.24 ml, 1.9 mmol) and acetic acid (170 mg, 2.83 mmol) in ethanol (2 ml) was added dropwise at room temperature. The reaction mixture was stirred overnight, then 25%. aq. ammonium hydroxide solution (0.39 ml) was added, and volatile material was removed by rotary evaporation. The residue was purified by chromatography (SiO2; CH2Cl2/MeOH/NH4OH 80:20:0.25) to afford the title compound (160 mg, 60%). Light brown oil, MS (ISP) −342.1 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063042B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-4f2e1e1ecd454331b83e5916560f9a76
Quellennotizuspto-grants-2011_11