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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914081Generated: November 2, 2026

4-Amino-1-methylpiperidine → HCID 25253676, compound

https://huagongshe.com/reaction/914081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 67117789HCID 67117789—
ProductHCID 25253676HCID 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, 11H) 1.86-2.09 (m, 5H) 2.15 (s, 3H) 2.63-2.81 (m, 2H) 3.57-3.79 (m, 1H) 3.94-4.16 (m, 2H) 4.81 (t, J=8.1 Hz, 1H) 7.32-7.46 (m, 1H) 7.51 (t, J=8.6 Hz, 1H) 7.85 (br. s., 1H) 7.88 (dd, J=4.3, 2.3 Hz, 1H) 8.30 (s, 1H) 9.88 (s, 1H). [M+H] calc'd for C26H32F3N7O2, 532. found 532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-73202e85e35b4c199ce349bee90b21ed
Source noteuspto-grants-2011_09