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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880970Generated: October 30, 2026

4-Amino-1-methylpiperidine → HCID 57955668, compound

https://huagongshe.com/reaction/1880970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantHCID 57955621HCID 57955621—
ProductHCID 57955668HCID 57955668—

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)-3-fluoro-5-methoxybenzoic acid and 1-methylpiperidin-4-amine as described in the General procedure for amide bond synthesis. The final compound was purified by reverse phase HPLC and basified to give the free base. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.33 (m, 4 H) 1.58 (d, J=14.4 Hz, 6 H) 1.75 (m, 2 H) 1.93 (m, 2 H) 1.99 (s, 1 H) 2.16 (s, 3 H) 2.78 (d, J=10.6 Hz, 2 H) 3.29 (s, 3 H) 3.83 (s, 2 H) 3.89-4.01 (t, J=12 Hz, 2 H) 4.32 (m, 1 H) 7.24-7.48 (m, 2 H) 8.10 (s, 1 H) 8.26 (d, J=7.6 Hz, 1 H) 8.53 (s, 1 H). [M+H] calc'd for C27H34F3N7O3, 562; found 562.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-6b5540dfdb314e6b8ec438792ea51007
Source noteuspto-grants-2012_11