HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine → (R)-5-(4-Methanesulfonyl-phenyl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine | HCID 71208609 | — |
| Reactant | (1-(Trifluoromethyl)cyclopropyl)methyl methanesulfonate | HCID 86649942 | — |
| Product | (R)-5-(4-Methanesulfonyl-phenyl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridine | HCID 71598834 | — |
Reaction Steps
The title compound is prepared from (R)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and methanesulfonic acid (1-trifluoromethyl-cyclopropyl)methyl ester following a procedure analogous to that described for Example 2. LC (method 1): tR=1.09 min; Mass spectrum (ESI+): m/z=481 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853239B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-b3ac2964173e4941abc84e5f100be2af |
| Source note | uspto-grants-2014_10 |