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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872210Generated: October 27, 2026

(R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine → (R)-4-[(R)-5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-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/872210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridineHCID 71208337—
ReactantCarbonic acid 4-nitro-phenyl ester (R)-2,2,2-trifluoro-1-methyl-ethyl esterHCID 86704996—
Product(R)-4-[(R)-5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid 2,2,2-trifluoro-1-methyl-ethyl esterHCID 90019268—

Reaction Steps

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-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=0.97 min; Mass spectrum (ESI+): m/z=504 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975277B2
Source datasetuspto-grants-2015_03
ORD IDord-7ffa335a669a41c4b66202cf2c6cf78d
Source noteuspto-grants-2015_03