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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 872209Erstellt: 27. Oktober 2026

(R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine → (R)-4-[(R)-5-(4-Methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid 2,2,2-trifluoro-1-methyl-ethyl ester

https://huagongshe.com/reaction/872209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridineHCID 71208609—
EduktCarbonic acid 4-nitro-phenyl ester (R)-2,2,2-trifluoro-1-methyl-ethyl esterHCID 86704996—
Produkt(R)-4-[(R)-5-(4-Methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid 2,2,2-trifluoro-1-methyl-ethyl esterHCID 90050904—

Reaktionsschritte

The title compound is prepared from (R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and carbonic acid 4-nitro-phenyl ester (R)-2,2,2-trifluoro-1-methyl-ethyl ester following a procedure analogous to that described for Example 1. LC (method 2): tR=1.07 min; Mass spectrum (ESI+): m/z=499 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08975277B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-0eb4c24d9fc4491780d243362d3db79d
Quellennotizuspto-grants-2015_03