HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-{1-[benzyl(methyl)amino]-propyl}-5-(trifluoromethyl)benzyl]-N-[3,5-bis(trifluoromethyl)-benzyl]-2-methyl-2H-tetrazol-5-amine | HCID 58966437 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[3,5-bis(trifluoromethyl)benzyl]-2-methyl-N-{2-[1-(methyl-amino)propyl]-5-(trifluoromethyl)benzyl}-2H-tetrazol-5-amine | HCID 58966411 | 109% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383660B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-e696dddc2e264a769428064a1ab4c03e |
| Source note | uspto-grants-2013_02 |