HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876101Generated: October 25, 2026
N-Methyl-4-anisidine → 1-Isoquinolinamine, N-(4-methoxyphenyl)-N-methyl-
https://huagongshe.com/reaction/1876101
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methyl-4-anisidine | HCID 22250 | — |
| Reactant | Isoquinoline, 1-chloro- | HCID 140539 | — |
| Product | 1-Isoquinolinamine, N-(4-methoxyphenyl)-N-methyl- | HCID 11300052 | 57% |
Reaction Steps
A mixture of 1-chloroisoquinoline (50 mg, 0.31 mmol) and (4-methoxy-phenyl)-methyl amine (300 mg, 2.2 mmol) was heated in a sealed tube at 140° C. overnight. The crude product was purified by chromatography (5-6% ethyl acetate/hexanes) on silica gel to give the title compound (46 mg, 0.17 mmol, 57%). 1H NMR (CDCl3): 8.22 (d, 1H, 5.7), 7.68 (d, 1H, J=8.1), 7.62 (d, 1H, J=8.7), 7.47 (ddd, 1H, J=0.9, 6.9, 8.1), 7.24 (d, 1H, J=6.0), 7.19 (ddd, 1H, J=1.5, 6.9, 8.7), 6.94 (m, 2H), 6.79 (m, 2H), 3.76 (s, 3H), 3.52 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309562B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-7d191d93287e407f8a465f760f1f5936 |
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| Source note | uspto-grants-2012_11 |
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