HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(1-Methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridine → 5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(1-Methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridine | HCID 67973503 | — |
| Reactant | (1-(Trifluoromethyl)cyclopropyl)methyl methanesulfonate | HCID 86649942 | — |
| Product | 5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridine | HCID 71598653 | — |
Reaction Steps
The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-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 3): tR=0.67 min; Mass spectrum (ESI+): m/z=486 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853239B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-64a3a0e5c372493c98a024a3c3e9d90f |
| Source note | uspto-grants-2014_10 |