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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914058Generated: October 25, 2026

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → HCID 25252907, compound

https://huagongshe.com/reaction/914058

Reaction equation

Participants

RoleNameHCIDCharge
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[5,4-b][1,4]diazepin-2-ylamino)-3-methoxybenzoic acidHCID 25252905—
Reactant1-Methylazetidin-3-amine xhydrochlorideHCID 67050583—
ProductHCID 25252907HCID 25252907—

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[5,4-b][1,4]diazepin-2-ylamino)-3-methoxybenzoic acid as described in the General procedure for amide bond synthesis using HATU and 1-methylazetidin-3-amine hydrochloride. The final compound was purified by reverse phase HPLC and basified to give the free base. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.58-1.71 (m, 7H) 1.90 (m, 3H) 2.42 (s, 3H) 3.32 (s, 3H) 3.76 (t, J=7.2 Hz, 2H) 3.94 (s, 3H) 4.05 (t, J=13.8 Hz, 2H) 4.38-4.60 (m, 1H) 4.76 (d, J=7.8 Hz, 1H) 7.35-7.59 (m, 2H) 7.99 (s, 1H) 8.26 (s, 1H) 8.29 (d, J=8.3 Hz, 1H) 8.72 (d, J=6.6 Hz, 1H). Melting point: 157-162° C. [M+H] calc'd for C25H31F2N7O3, 516. found 516.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-9209bb94c67948c0ab24902e558550ca
Source noteuspto-grants-2011_09