HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989037Generated: October 26, 2026
1-Chloro-3-(2-trifluoromethyl-phenyl)-isoquinoline → HCID 178506126, compound
https://huagongshe.com/reaction/989037
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-3-(2-trifluoromethyl-phenyl)-isoquinoline | HCID 21939226 | — |
| Reactant | HCID 178418311 | HCID 178418311 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178506126 | HCID 178506126 | 4% |
Reaction Steps
A solution of 1-chloro-3-(2-trifluoromethyl-phenyl)-isoquinoline (0.326 mmol) and 1H-[1,2,4]triazol-3-ylamine (0.651 mmol) in ethanol (3 mL) was heated at 160° C. and the solvent evaporated with a stream of nitrogen. The remaining oil was then heated at 160° C. for 18 hours under nitrogen. The resulting melt was dissolved in 5% methanol/dichloromethane (50 mL), washed with saturated aqueous sodium bicarbonate (1×25 mL) then dried over magnesium sulfate. Purification by silica gel chromatography afforded IX-175 as a colorless oil (4% yield). 1H NMR (500 MHz, CDCl3) δ9.18 (d, 1H), 8.82 (s, 1H), 7.90 (d, 1H), 7.85-7.75 (m, 3H), 7.71-7.62 (m, 3H), 7.60-7.55 (m, 2H), 4.42-4.35 (m, 1H). LC−MS (ES+) 356.16 (M+H); HPLC-Method D, Rt 3.55 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638926B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-15603e9c205d46d38d1a7a249a009198 |
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| Source note | uspto-grants-2003_10 |
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