HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900317Generated: October 30, 2026
3-Methoxyaniline → 5-((4-aminopiperidin-1-yl)methyl)-N-(3-methoxyphenyl) quinazolin-4-amine
https://huagongshe.com/reaction/900317
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | N-((4-chloroquinazolin-5-yl)methyl)-N,N-diethylethanaminium bromide | HCID 86607964 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-((4-aminopiperidin-1-yl)methyl)-N-(3-methoxyphenyl) quinazolin-4-amine | HCID 11847597 | 17.3% |
Reaction Steps
A mixture of 14A (80 mg, 0.223 mmol) and 3-methoxyaniline (18.6 mg, 0.151 mmol) in CH3CN (1.5 ml) was heated at 55° C. for 2 h. After cooling to room temperature, 4-N-Boc-aminopiperidine (300 mg, 1.5 mmol) was added and the mixture was heated at 60° C. overnight. The reaction mixture was concentrated in vacuo and the residue was purified by prep HPLC. The desired fraction was concentrated and the resulting residue was dissolved in a mixture of TFA/DCM (1 ml/1 ml) and stirred at room temperature for 1 h, then concentrated. The residue was purified by SCX column, followed by silica gel flash column (DCM/MeOH/NH4OH=90/10/1) to give 14B (9.5 mg, 17%). The compound has an analytical HPLC retention time=1.288 min (Chromolith SpeedROD column 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA over 4 minutes, 4 mL/min, monitoring at 254 nm) and a LC/MS M++H=364+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358256B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-33e3c35bc3b9474491a8b649f696d068 |
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| Source note | uspto-grants-2008_04 |
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