HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724926Generated: October 30, 2026
4-Methoxybenzylamine → 2-(4-methoxybenzylamino)-5,11-dihydro-11-ethyl-8-[2-(4-pyridyl)ethyl]-5-methyl-6-H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
https://huagongshe.com/reaction/724926
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 5-Chloro-2-ethyl-9-methyl-13-[2-(pyridin-4-yl)ethyl]-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-10-one | HCID 470666 | — |
| Product | 2-(4-methoxybenzylamino)-5,11-dihydro-11-ethyl-8-[2-(4-pyridyl)ethyl]-5-methyl-6-H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 19711107 | 26% |
Reaction Steps
A mixture of 2-chloro-5,11-dihydro-11-ethyl-8-[2-(4-pyridyl)ethyl]-5-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (0.285 g, 0.7 mmol) and 4-methoxybenzylamine (0.23 mL, 1.8 mmol) in 4 mL of xylenes was heated at 150° C. in a sealed tube. After 24 hours, additional amine (0.23 mL, 1.8 mmol) was added and the reaction temperature was increased to 250° C. Heat was removed after 2d, and the reaction mixture was washed with saturated aqueous ammonium chloride to remove excess amine. The organic layer was dried (magnesium sulfate) and concentrated. Purification by flash chromatography (elution with methanol-dichloromethane) afforded the title compound (0.09 g, 26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05705499 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-41211b93722a4cc091d3e939ae59cce8 |
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| Source note | uspto-grants-1998_01 |
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