HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18125Generated: October 25, 2026
Diethyl Ether → 5-((4-Chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)indolin-2-one
https://huagongshe.com/reaction/18125
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Amino-2-oxindole | HCID 2773213 | — |
| Reactant | 2,4-Dichloro-5-(trifluoromethyl)pyrimidine | HCID 2782774 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tert-butyl alcohol 1,2-dichloroethane | HCID 21868497 | — |
| Product | 5-((4-Chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)indolin-2-one | HCID 21923104 | — |
Reaction Steps
To a solution of 5-trifluoromethyl-2,4-dichloropyrimidine (214.8 g; 0.921 mol) in 1:1 DCE/tBuOH (1.240 L) was added Zinc chloride 1M solution in ether (1 eq; 0.921 L). After 0.5 hour, 5-amino-oxindole (124 g; 0.837 mol) was added followed by triethylamine (129.4 ml; 0.921 mol) keeping temperature at 25° C. The reaction was allowed to stir at room temperature overnight, then was concentrated and the product triturated from methanol as a yellow solid (224.3 g; 82%). 1H NMR (DMSO-d6, 400 MHz) 3.29 (s, 2H), 6.76 (d, J=7.9 Hz, 2H), 7.39 (d, J=8.3 Hz), 7.51 (br s, 1H), 8.71 (s, 1H), 10.33 (s, 1H), 10.49 (s, 1H). 13C NMR (DMSO-d6, 100 MHz) δ 177.0, 161.3, 158.7 (br), 140.7, 132.8, 126.9, 123.7 (q, J=268 Hz), 121.0, 118.7, 111.2 (q, J=32 Hz), 109.6, 36.7; HPLC ret. time: 5.759 min. LRMS (M+) 329.1, 331.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741336B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-31f12368ebb64b7d97c158f30cacfd86 |
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| Source note | uspto-grants-2010_06 |
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