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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898377Generated: October 26, 2026

Water → HCID 178425051, compound

https://huagongshe.com/reaction/1898377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178425067HCID 178425067—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventThionyl ChlorideHCID 24386—
ProductHCID 178425051HCID 1784250518.7%

Reaction Steps

To a solution of 2-[(2-chloro-6-methylphenyl)amino]-7,7-dimethyl-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxylic acid (Intermediate-35, 0.100 g, 0.268 mmol) in benzene (2 mL), thionyl chloride (3.0 mL) was added at 5-10° C. and the reaction mass was refluxed for 3 h. To the reaction mixture, stirred solution of 4-trifluoromethyl phenyl amine (0.065 g, 0.403 mmol) and DIPEA (0.069 g, 0.534 mmol) in THF (10.0 mL) for 1 h at RT under N2-atmosphere was added and stirring was continued for another 1 h at RT. Excess of thionyl chloride was co-evaporated with THF under vacuum. Water was added to the reaction mass and it was extracted with ethyl acetate. The organic layer was separated, dried over anhydrous sodium sulphate and concentrated. The obtained crude product was purified by column chromatography on neutral alumina eluting with 0.7-1.0% MeOH:DCM to afford 0.012 g of the desired product. 1HNMR (DMSO-d6): δ 1.58 (s, 6H), 2.24 (s, 3H), 3.44 (s, 2H), 7.25-7.31 (m, 2H), 7.42 (d, J=7.2 Hz, 1H), 7.50 (s, 1H), 7.70 (d, J=8.7 Hz, 2H), 7.91 (d, J=8.4 Hz, 2H), 9.09 (s, 1H), 10.01 (s, 1H), 10.94 (s, 1H); MS [M−H]−: 513.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-c74b73b08b7a4b41ade320601ecf11c5
Source noteuspto-grants-2013_08