HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898391Generated: November 2, 2026
3-(Trifluoromethyl)aniline → HCID 178425401, compound
https://huagongshe.com/reaction/1898391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178425402 | HCID 178425402 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178425401 | HCID 178425401 | 16.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519149B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e2aeb04798984a66a39d2040ec15aac3 |
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| Source note | uspto-grants-2013_08 |
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