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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390742Generated: October 29, 2026

Morpholine → N-[3,5-Bis(trifluoromethyl)benzyl]-2-methyl-N-[2-(1-morpholin-4-ylethyl)-5-(trifluoromethyl)benzyl]-2H-tetrazol-5-amine

https://huagongshe.com/reaction/390742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant2-{[(3,5-bis-trifluoromethyl-benzyl)(2-methyl-2H-tetrazol-5-yl)amino]-methyl}-4-trifluoromethyl-benzaldehydeHCID 58966524—
ReactantHCID 178418385HCID 178418385—
SolventEthanolHCID 702—
ProductN-[3,5-Bis(trifluoromethyl)benzyl]-2-methyl-N-[2-(1-morpholin-4-ylethyl)-5-(trifluoromethyl)benzyl]-2H-tetrazol-5-amineHCID 5896650928%

Reaction Steps

To a solution of benzotriazole (12.8 mg, 0.1075 mmoles) in ethanol (2 mL) was added morpholine (9.4 mg, 0.1075 mmoles) and the reaction was stirred for 10 minutes. A solution of 2-{[(3,5-bis-trifluoromethyl-benzyl)-(2-methyl-2H-tetrazol-5-yl)-amino]-methyl}-4-trifluoromethyl-benzaldehyde (50 mg, 0.0977 mmoles) in ethanol (1 mL) was added to the reaction mixture and it was further stirred for 16 hours. The imine fragment was observed MH+=581.4. Parent ion for the intermediate was not found. The ethanol was evaporated and the crude product was taken to the next step. Half of the crude was dissolved in toluene and methyl magnesium bromide (97 □L, 0.2916 mmoles of a 3M solution in ether) was added. The reaction mixture was heated at reflux for 2 hours. LC-MS indicated formation of product. The solvent was evaporated from the reaction mixture. 1N NaOH solution was added and the aqueous layer was extracted with dichloromethane. The organic layer was concentrated and the residue was dissolved in DMSO and purified on prepHPLC (Shimadzu, 30×50 C18, Basic, 30-95%, 0.1% NaOH, 8 min gradient, 220 UV) to yield 8.2 mg (28%) of the title compound as clear oil. MS (ES+) Calc: 596.4, Found: 597.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383660B2
Source datasetuspto-grants-2013_02
ORD IDord-4be07b88af3a4ed19241713e1ea64f70
Source noteuspto-grants-2013_02