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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390745Generated: October 30, 2026

N-[2-{1-[benzyl(methyl)amino]-propyl}-5-(trifluoromethyl)benzyl]-N-[3,5-bis(trifluoromethyl)-benzyl]-2-methyl-2H-tetrazol-5-amine → N-[3,5-bis(trifluoromethyl)benzyl]-2-methyl-N-{2-[1-(methyl-amino)propyl]-5-(trifluoromethyl)benzyl}-2H-tetrazol-5-amine

https://huagongshe.com/reaction/390745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-{1-[benzyl(methyl)amino]-propyl}-5-(trifluoromethyl)benzyl]-N-[3,5-bis(trifluoromethyl)-benzyl]-2-methyl-2H-tetrazol-5-amineHCID 58966437—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductN-[3,5-bis(trifluoromethyl)benzyl]-2-methyl-N-{2-[1-(methyl-amino)propyl]-5-(trifluoromethyl)benzyl}-2H-tetrazol-5-amineHCID 58966411109%

Reaction Steps

To a Parr flask was added 20% Pd(OH)2 on carbon (23.2 mg) followed by addition of methanol (22 mL). To this suspension was added a solution N-[2-{1-[benzyl(methyl)amino]-propyl}-5-(trifluoromethyl)benzyl]-N-[3,5-bis(trifluoromethyl)-benzyl]-2-methyl-2H-tetrazol-5-amine (298.7 mg, 0.463 mmoles) in methanol. The reaction mixture was stirred under hydrogen (pressure =14.7 psi) at room temperature for 9 hours. The reaction mixture was filtered through Celite, washed with methanol, concentrated under vacuo to give 279.8 mg (100%) of the title compound as yellow oil. MS (ES+) Calc: 608.5, Found: 609.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383660B2
Source datasetuspto-grants-2013_02
ORD IDord-e696dddc2e264a769428064a1ab4c03e
Source noteuspto-grants-2013_02