Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872214Generated: October 30, 2026

4-nitrophenyl (2S)-1,1,1-trifluoropropan-2-yl carbonate → (S)-4-[(R)-5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-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/872214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-nitrophenyl (2S)-1,1,1-trifluoropropan-2-yl carbonateHCID 68756210—
Reactant(R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridineHCID 89612048—
Product(S)-4-[(R)-5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid 2,2,2-trifluoro-1-methyl-ethyl esterHCID 90019550—

Reaction Steps

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and carbonic acid 4-nitro-phenyl ester (S)-2,2,2-trifluoro-1-methyl-ethyl ester following a procedure analogous to that described in Example 1. LC (method 2): tR=0.92 min; Mass spectrum (ESI+): m/z=518 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975277B2
Source datasetuspto-grants-2015_03
ORD IDord-c75c9c495a0145cf9a1ce91f21501e55
Source noteuspto-grants-2015_03