HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydropyran-4-ylacetic acid → HCID 72191468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydropyran-4-ylacetic acid | HCID 2773575 | — |
| Reactant | 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid | HCID 10988214 | — |
| Reactant | tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate | HCID 22181157 | — |
| Product | HCID 72191468 | HCID 72191468 | — |
Reaction Steps
The title compound was prepared as described in Example 1A, substituting N-(4-(piperidin-4-yloxy)phenyl)-1-(pyridin-3-yl)azetidine-3-carboxamide for tert-butyl 4-(4-aminophenoxy)piperidine-1-carboxylate and 2-(tetrahydro-2H-pyran-4-yl)acetic acid for 1-(benzyloxycarbonyl)azetidine-3-carboxylic acid. 1H NMR (300 MHz, DMSO-d6) δ ppm 9.95 (bs, 1H), 7.93 (d, J=4.2 Hz, 1H), 7.88-7.83 (m, 1H), 7.55-7.47 (m, 2H), 7.26-7.08 (m, 1H), 7.01-6.78 (m, 3H), 4.14-4.04 (m, 2H), 4.02-3.62 (m, 6H), 2.37-1.73 (m, 6H), 1.66-1.00 (m, 8H); MS (ESI(+)) m/e 479 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975398B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-2ea5baaee648483283d6a6af4351f43e |
| Source note | uspto-grants-2015_03 |