Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114811Generated: November 3, 2026

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → {Amino-[4-({3-[2-(2,4-dichloro-phenyl)-ethoxy]-4-methyl-benzoylamino}-methyl)-piperidin-1-yl]-methylene}-carbamic Acid Benzyl Ester

https://huagongshe.com/reaction/2114811

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—
Reactant3-[2-(2,4-Dichloro-phenyl)-ethoxy]-4-methyl-benzoic acidHCID 22052388—
ReactantHCID 69305786HCID 69305786—
SolventDimethylformamideHCID 6228—
Product{Amino-[4-({3-[2-(2,4-dichloro-phenyl)-ethoxy]-4-methyl-benzoylamino}-methyl)-piperidin-1-yl]-methylene}-carbamic Acid Benzyl EsterHCID 49823095—

Reaction Conditions

Temperature0 °C

Reaction Steps

97 mg of 3-[2-(2,4-Dichloro-phenyl)-ethoxy]-4-methyl-benzoic acid and 124.3 mg of [Amino-(4-aminomethyl-piperidin-1-yl)-methylene]-carbamic acid benzyl ester trifluoroacetic acid salt were dissolved in 5 ml of DMF. After cooling to 0° C. 136 mg of HATU and 106 mg of NEM were added. The mixture was stirred at 0° C. for 2 hours and at room temperature for 3 hours. The solvent was removed under reduced pressure and the residue was purified by preparative HPLC (C18 reverse phase column) (gradient acetonitrile water (containing 0.1% trifluoro-acetic acid) 90:10 to 0:100). The fractions containing the product were evaporated and lyophilized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435747B2
Source datasetuspto-grants-2008_10
ORD IDord-3e8d86efac234ab98b1d5d7e55df7140
Source noteuspto-grants-2008_10