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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898479Generated: November 1, 2026

3-(Trifluoromethyl)aniline → HCID 67503683, compound

https://huagongshe.com/reaction/1898479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantTrimethylaluminumHCID 16682925—
ReactantMethyl 2-((3,5-dichloropyridin-4-yl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylateHCID 67502200—
SolventTolueneHCID 1140—
ProductHCID 67503683HCID 6750368338.3%

Reaction Steps

The title compound was prepared following the procedure described for Example-143 by using methyl 2-((3,5-dichloropyridin-4-yl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate (Intermediate-60, 0.100 g, 0.237 mmol), 3-(trifluoromethyl) aniline (0.057 g, 0.356 mmol), trimethyl aluminium (2M solution in toluene) (0.5 mL), dry toluene (5.0 mL) to afford 0.050 g of the desired product. 1HNMR (DMSO-d6): δ 1.61 (s, 6H), 3.49 (s, 2H), 3.59 (s, 3H), 7.24 (s, 1H), 7.45 (d, J=7.8 Hz, 1H), 7.59 (t, J=7.8 Hz, 1H), 7.78 (d, J=8.4 Hz, 1H), 8.31 (s, 1H), 8.47 (s, 2H), 9.90 (s, 1H), 10.91 (s, 1H); MS [M]+: 550.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-0da28a40c03d4d8692717b055e57cbf4
Source noteuspto-grants-2013_08