HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-1-methylpiperidine → HCID 57955606, 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 67117794 | HCID 67117794 | — |
| Product | HCID 57955606 | HCID 57955606 | — |
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-methylbenzoic 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 1.36-1.77 (m, 11 H) 1.98 (m, 4 H) 2.16 (s, 3 H) 2.31 (s, 3 H) 2.75 (d, J=11 Hz, 2 H) 3.17 (br. s., 2 H) 3.67 (d, J=7 Hz, 1 H) 4.03 (t, J=14 Hz, 3 H) 4.81 (m, 1 H) 7.22 (d, J=8 Hz, 1 H) 7.46 (d, J=8 Hz, 1 H) 7.68 (br. s., 1 H) 7.99 (d, J=8 Hz, 1 H) 8.25 (s, 1 H) 9.51 (br. s., 1 H). [M+H] calc'd for C27H35F2N7O2, 528; found 528.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318727B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9f7bea883ab64d628d86d9e549441ee1 |
| Source note | uspto-grants-2012_11 |