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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898404Generated: October 30, 2026

4-(Trifluoromethyl)aniline → HCID 67503518, compound

https://huagongshe.com/reaction/1898404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
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 67503518HCID 675035187.3%

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, 0.2564 mmol), thionyl chloride (2.0 mL), 4-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 0.010 g of the desired product. 1HNMR (DMSO-d6): δ 1.61 (s, 6H), 3.47 (s, 3H), 3.56 (s, 2H), 7.17-7.01 (m, 1H), 7.21 (bs, 2H), 7.29 (d, J=8.4 Hz, 1H), 7.70 (d, J=8.4 Hz, 2H), 7.90 (d, J=7.8 Hz, 2H), 9.92 (bs, 1H), 10.52 (bs, 1H): MS [M+H]+: 533.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-5bf65ab98f9b4801abfe04f5a47bec18
Source noteuspto-grants-2013_08