HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218206Generated: November 1, 2026
Homoveratrylamine → HCID 178490293, compound
https://huagongshe.com/reaction/2218206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | 4-(2-chloro-9H-purin-6-yl)morpholine | HCID 3274603 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178490293 | HCID 178490293 | 74.8% |
Reaction Steps
As shown in Scheme 3 above, a mixture of 2,6-dichloropurine (1.90 g, 10 mmol) and morpholine (2.34 g, 30 mmol) in water (25 mL) was heated under reflux for 15 min. Solidified reaction mixture was cooled to room temperature. Solid was filtered out and washed with water, methanol and ether. The 2-chloro-6-morpholin-4-yl-9H-purine was obtained in 96% yield (2.30 g). A mixture of 2-chloro-6-morpholin-4-yl-9H-purine (1.92 g, 8 mmol) and 2-(3,4-dimethoxyphenyl)ethylamine (4.35 g, 24 mmol) in sealed tube and under nitrogen was stirred at 190-195° C. for 1 hour. The reaction mixture turned to clear solution initially and then formed a slurry. The reaction mixture was cooled to room temperature diluted with methanol (8 mL) and the solid was collected by filtration, washed with methanol and Et2O and dried to afford 2.30 g (74% yield) of [2-(3,4-dimethoxy-phenyl)-ethyl]-(6-morpholin-4-yl-9H-purin-2-yl)amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410990B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-31c1aedeb65f4df29cdbfd8dfb7a3867 |
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| Source note | uspto-grants-2008_08 |
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