HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435739Generated: October 30, 2026
4-Chloro-N-methylbenzenamine → HCID 9925034, compound
https://huagongshe.com/reaction/1435739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-N-methylbenzenamine | HCID 70272 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 83240562 | HCID 83240562 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9925034 | HCID 9925034 | 22% |
Reaction Steps
A mixture of 4-chloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazin-2-yl-amine (106 mg, 0.42 mmol), (4-chloro-phenyl)-methyl-amine (0.15 ml, 1.25 mmol), tetrahydrofuran (5 ml), and diisopropylethylamine (0.75 ml, 4.2 mmol) was heated at 40° C. for 72 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in dichloromethane (25 ml). The solution was washed with hydrochloric acid (1 M, 25 ml) and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with 2% methanol-dichloromethane followed by 5% methanol-dichloromethane. Recrystallization (ethyl acetate-hexane) provided the title compound (33 mg, 22% yield). 1H NMR (DMSO-d6) 7.78 (s, 1H), 7.37-7.46 (m, 4H), 7.26 (d, J=8.4 Hz, 1H), 7.10 (br s, 2H), 3.43 (s, 3H), 2.37 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618968B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-682b5e661728461c8974931673772162 |
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| Source note | uspto-grants-2009_11 |
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