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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2410366Erstellt: 24. Oktober 2026

Diisopropylethylamine → Methyl 1-({4-[({4-[(trans-2-Hydroxycyclopentyl)oxy]-1,2-benzisoxazol-3-yl}oxy)methyl]piperidin-1-yl}methyl)cyclopentanecarboxylate

https://huagongshe.com/de/reaction/2410366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethyl 1-(iodomethyl)cyclopentanecarboxylateHCID 67231596—
Edukttrans-2-{[3-(Piperidin-4-ylmethoxy)-1,2-benzisoxazol-4-yl]oxy}cyclopentanolHCID 69316225—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktMethyl 1-({4-[({4-[(trans-2-Hydroxycyclopentyl)oxy]-1,2-benzisoxazol-3-yl}oxy)methyl]piperidin-1-yl}methyl)cyclopentanecarboxylateHCID 6931898611%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of trans-2-{[3-(piperidin-4-ylmethoxy)-1,2-benzisoxazol-4-yl]oxy}cyclopentanol (77 mg, 0.23 mmol, EXAMPLE 33, Step 2), methyl 1-(iodomethyl)cyclopentanecarboxylate (75 mg, 0.28 mmol, EXAMPLE 33, Step 1), and N,N-diisopropylethylamine (0.12 mL, 0.70 mmol) in N-methylpyrrolidone (3.0 mL) was heated at 120° C. for 14 h. The mixture was cooled to room temperature and the mixture was diluted with ethyl acetate and water. The mixture was extracted with ethyl acetate (30 mL×2) and washed with brine. The extracts were combined and dried over sodium sulfate and concentrated in vacuo to give a brown solid. The residual solid was purified by silica gel column chromatography (hexane/ethyl acetate 3:2) to give 12 mg (11%) of the title compound as a colorless viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08816090B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-8b5dfdba53364787aa62430ea025b484
Quellennotizuspto-grants-2014_08