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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525459Erstellt: 25. Oktober 2026

4-Piperidineacetic acid → HCID 60162961, Verbindung

https://huagongshe.com/reaction/525459

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Piperidineacetic acidHCID 1512594—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-ethyl-piperidine-4-carboxylic acidHCID 60162828—
Edukt6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehydeHCID 86668412—
ProduktHCID 60162961HCID 6016296160%

Reaktionsschritte

The compound was prepared in a manner similar as to that described for 1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-ethyl-piperidine-4-carboxylic acid using Piperidin-4-yl-acetic acid (0.0554 g, 0.387 mmol), 6-(4-tert-Butyl-cyclohexyloxy)-naphthalene-2-carbaldehyde (0.100 g, 0.322 mmol) and Sodium triacetoxyborohydride (0.212 g, 0.9 mol) to give 85 mg {1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-piperidin-4-yl}-acetic acid (60%). ESI-LCMS (438 M+H). 1H NMR (DMSO-d6, 400 MHz): Shift (ppm) 7.71-8.01 (m, 3H), 7.43 (d, J=2.0 Hz, 2H), 7.10-7.30 (m, 1H), 4.38 (d, J=4.8 Hz, 3H), 3.28-3.55 (m, 2H), 2.82-3.14 (m, 2H), 2.20 (d, J=6.3 Hz, 4H), 1.85 (br. s., 5H), 1.38 (br. s., 7H), 0.89 (s, 9H)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340527B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-a914696fb58b4be9980dfab23fa814b7
Quellennotizuspto-grants-2016_05