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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898405Generated: October 31, 2026

3-(Trifluoromethyl)aniline → HCID 67503476, compound

https://huagongshe.com/reaction/1898405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylic AcidHCID 67502720—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67503476HCID 6750347611%

Reaction Steps

The title compound was prepared by following the procedure as described for Example-108 using 2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylic acid (Intermediate-49, 0.100 g, 0.256 mmol), thionyl chloride (2.0 mL), 3-trifluoromethyl aniline (0.124 g, 0.769 mmol), THF (5.0 mL) and DIPEA (2 mL). The obtained crude product was purified by column chromatography on basic alumina eluting with 0.7-1.0% MeOH:DCM to afford 0.015 g of the desired product. 1HNMR (DMSO-d6): δ 1.61 (s, 6H), 3.46 (s, 2H), 3.56 (s, 3H), 7.00 (m, 1H), 7.20 (m, 2H), 7.28 (d, 2H), 7.28 (d, 1H), 7.45 (d, 1H), 7.56 (t, 1H), 7.75 (d, J=7.2 Hz, 1H), 8.31 (s, 1H), 9.98 (s, 1H), 10.51 (s, 1H); MS [M+H]+: 533.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-507aa92df7dd49cf8264532cff742196
Source noteuspto-grants-2013_08