HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375498Generated: October 29, 2026
3-(Trifluoromethyl)aniline → 1-[(5-Chloro-2-thienyl)methyl]-3-{[3-(trifluoromethyl)phenyl]imino}1,3-dihydro-2H-indol-2-one
https://huagongshe.com/reaction/2375498
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | 1-(5-Chloro-thiophen-2-yl-methyl)-1h-indole-2,3-dione | HCID 22022439 | — |
| Product | 1-[(5-Chloro-2-thienyl)methyl]-3-{[3-(trifluoromethyl)phenyl]imino}1,3-dihydro-2H-indol-2-one | HCID 10070782 | 61% |
Reaction Steps
A mixture of 1-[(5-chloro-2-thienyl)methyl]-2H-indole-2,3-dione (25 mg, 0.09 mmol) (prepared as described below) and 3-trifluoromethylaniline (11.3 μL, 0.09 mmol) was heated neat at 140° C. for 2 h. The crude material was purified by preparative TLC using a mixture of 3:7 ethyl acetate in hexane as the eluent, giving the desired product (23 mg 0.05 mmol, 61%). 1H NMR (400 MHz): δ (major isomer) 7.57 (t, J=7.7, 1H), 7.53 (t, J=7.8, 1H), 7.33 (t, J=7.8, 1H), 7.28 (s, 1H), 7.19 (d, J=7.6, 2H), 6.94-6.72 (m, 4H), 6.56 (d, J=7.7, 1H), 5.02 (s, 2H); ESI-MS m/z found 421 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465750B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-e55ea8e85d92446c892a3a0b882d08ee |
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| Source note | uspto-grants-2008_12 |
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