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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075050Generated: November 1, 2026

Ammonia → HCID 58968747, compound

https://huagongshe.com/reaction/2075050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58968730HCID 58968730—
SolventDichloromethaneHCID 6344—
ProductHCID 58968747HCID 5896874734%

Reaction Steps

To a solution of N-(2-(methoxy(piperidin-4-yl)methyl)-5-(trifluoromethyl)benzyl)-N-(3,5-bis(trifluoromethyl)benzyl)-2-methyl-2H-tetrazol-5-amine (19.4 mg, 0.032 mmol) in methylene chloride (0.5 mL) at room temperature was added Hunig's base (8.9 mg, 12 μL, 0.069 mmol) followed by phosgene in toluene (20%, 25 μL, 0.048 mmol). The mixture was stirred at room temperature for 3 hours. Ammonia in ethanol (1 mL) was added and the mixture was stirred at room temperature overnight. Solvent was removed in vacuo The residue was purified by chromatography over 12+S Biotage silica column (eluted with 0-50% ethyl acetate in hexane) to afford the title compound (7.4 mg, 34%). 1H NMR (400 MHz, CDCl3) δ ppm 1.11-1.18(m, 1H) 1.20-1.31 (m, 2H) 1.24(t, J=7.05 Hz, 3H) 1.61-1.71 (m, 1H) 1.85(d, J=12.86 Hz, 1H) 2.56 (q, J=14.94 Hz, 2H) 3.04 (s, 3H) 4.05-4.19 (m, 2H) 4.10 (q, J=7.05 Hz, 2H) 4.16 (d, J=7.05 Hz, 1H) 4.21 (s, 3H) 4.68 (d, J=15.77 Hz, 1H) 4.71 (s, 2H) 4.88 (d, J=15.77 Hz, 1H) 7.36 (s, 1H) 7.50 (d, J=7.88 Hz, 1H) 7.58 (d, J=8.71 Hz, 1H) 7.64 (s, 2H) 7.78 (s, 1H). MS (ES+) Calc: 682.6, Found: 683.6 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919506B2
Source datasetuspto-grants-2011_04
ORD IDord-c864bacb11ae4dca894ffea7aaff5adb
Source noteuspto-grants-2011_04