HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668942Generated: October 29, 2026
3-(Trifluoromethoxy)aniline → HCID 67338962, compound
https://huagongshe.com/reaction/1668942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethoxy)aniline | HCID 73753 | — |
| Reactant | 4-Chloro-8-iodo-2,7-dimethylquinazoline | HCID 58466465 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 67338962 | HCID 67338962 | 74.1% |
Reaction Steps
4-Chloro-8-iodo-2,7-dimethylquinazoline (0.30 g, 0.94 mmol) and 3-(trifluoromethoxy)benzenamine (0.20 g, 1.1 mmol) were placed in a microwave vial containing 3 mL of IPA. The vial was capped and heated in a microwave reactor at 170° C. for 10 min. The mixture was concentrated in vacuo and the residue was taken up in ethyl acetate and washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was dried with sodium sulfate, concentrated and purified by column chromatography on silica gel using a gradient of 20 to 60% EtOAc in hexanes to give a 8-iodo-2,7-dimethyl-N-(3-(trifluoromethoxy)phenyl)quinazolin-4-amine (0.32 g, 74%) as an off-white solid. MS (M+H)+ 460.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989461B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-9bb9efe741c84c248e1675acc9f08a8f |
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| Source note | uspto-grants-2011_08 |
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