HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-1-methylpiperidine → HCID 25253676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 67117789 | HCID 67117789 | — |
| Product | HCID 25253676 | HCID 25253676 | — |
Reaction Steps
The title compound was synthesized from 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-2-fluorobenzoic acid as described in the General procedure for amide bond synthesis using HATU and 1-methylpiperidin-4-amine. The final compound was purified by reverse phase HPLC and basified to give the free base 1H NMR (400 MHz, DMSO-d6) δ ppm 1.44-1.74 (m, 11 H) 1.86-2.09 (m, 5 H) 2.15 (s, 3 H) 2.63-2.81 (m, 2 H) 3.57-3.79 (m, 1 H) 3.94-4.16 (m, 2 H) 4.81 (t, J=8.1 Hz, 1 H) 7.32-7.46 (m, 1 H) 7.51 (t, J=8.6 Hz, 1 H) 7.85 (br. s., 1 H) 7.88 (dd, J=4.3, 2.3 Hz, 1 H) 8.30 (s, 1 H) 9.88 (s, 1 H). [M+H] calc'd for C26H32F3N7O2, 532; found 532.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318727B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-7235f6c00edc4eea9311d3579f886ba0 |
| Source note | uspto-grants-2012_11 |