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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912514Generated: November 4, 2026

3-amino-2-(trifluoromethyl)-4(3H)-quinazolinone → 2-[(1S,2S,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-yl]-N-[4-oxo-2-(trifluoromethyl)quinazolin-3(4H)-yl]acetamide

https://huagongshe.com/reaction/1912514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-amino-2-(trifluoromethyl)-4(3H)-quinazolinoneHCID 1488531—
ReactantHCID 86665150HCID 86665150—
Product2-[(1S,2S,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-yl]-N-[4-oxo-2-(trifluoromethyl)quinazolin-3(4H)-yl]acetamideHCID 68749701—

Reaction Steps

The product from Example 1C and 3-amino-2-(trifluoromethyl)quinazolin-4(3H)-one (Bionet) were processed using method analogous to that described in Example 1D to afford the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.00 (d, J=9.8 Hz, 1H) 1.08 (s, 3H) 1.23 (d, J=5.1 Hz, 3H) 1.85-2.05 (m, 5H) 2.06-2.24 (m, 1H) 2.31-2.45 (m, 2H) 2.53-2.61 (m, 2H) 2.62-2.76 (m, 1H) 7.58 (s, 1H) 7.60-7.68 (m, 1H) 7.88 (d, J=3.7 Hz, 1H) 8.31 (d, J=7.8 Hz, 1H); MS (ESI+) m/z 394 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609674B2
Source datasetuspto-grants-2013_12
ORD IDord-fc4fa05735b34c409d88e2df89157b54
Source noteuspto-grants-2013_12