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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898391Generated: November 2, 2026

3-(Trifluoromethyl)aniline → HCID 178425401, compound

https://huagongshe.com/reaction/1898391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178425402HCID 178425402—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178425401HCID 17842540116.5%

Reaction Steps

The title compound was prepared by following the procedure described for Example-108 using 2-[(2-chloro-5-methylphenyl)amino]-7,7-dimethyl-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxylic acid (Intermediate-27, 0.175 g, 0.471 mmol), thionyl chloride (2.0 mL), 3-trifluoromethyl phenyl amine (0.114 g, 0.707 mmol), THF (5.0 mL) and DIPEA (2 mL). The obtained crude product was purified by column chromatography on neutral alumina eluting with 0.9% MeOH:DCM to afford 0.040 g of the desired product. 1HNMR (DMSO-d6): δ 1.61 (s, 6H), 2.33 (s, 3H), 3.16 (d, J=5.4 Hz, 2H), 6.87-6.88 (m, 1H), 7.35 (d, J=8.4 Hz, 1H), 7.44 (d, J=7.2 Hz, 1H), 7.60 (t, J=7.8 Hz, 1H), 7.73 (s, 1H), 7.78 (d, J=7.8 Hz, 1H), 8.34 (s, 2H), 9.00 (s, 1H), 10.01 (s, 1H), 10.05 (s, 1H); MS [M+H]+: 515.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-e2aeb04798984a66a39d2040ec15aac3
Source noteuspto-grants-2013_08