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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914079Generated: October 25, 2026

4-Amino-1-methylpiperidine → 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-methyl-N-(1-methylpiperidin-4-yl)benzamide

https://huagongshe.com/reaction/914079

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—
Reactant4-(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-methyl-benzoic acidHCID 58015032—
Product4-(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-methyl-N-(1-methylpiperidin-4-yl)benzamideHCID 25253528—

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-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 1.42-2.04 (m, 16H) 2.10-2.22 (m, 3H) 2.29 (s, 3H) 2.77 (d, J=11.1 Hz, 2H) 3.72 (dd, J=7.3, 4.0 Hz, 1H) 3.98 (t, J=14.0 Hz, 2H) 4.60 (t, J=8.2 Hz, 1H) 7.64 (d, J=8.3 Hz, 1H) 7.68-7.80 (m, 2H) 8.08 (d, J=7.8 Hz, 1H) 8.19 (s, 1H) 8.60 (s, 1H). [M+H] calc'd for C27H35F2N7O2, 528. found 528.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-e22342d9fca14ab28f578bdaf239eb08
Source noteuspto-grants-2011_09