Water → HCID 9993837、化合物

2.5 g of N-methyl-(2-(3,4-dimethoxyphenyl)ethyl)amine was dissolved in 25 ml of N,N-dimethylformamide, followed by the addition of 1.95 g of anhydrous potassium carbonate and 1.65 ml of 4-bromovaleronitrile. The obtained mixture was reacted at a room temperature for 16 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and a saturated aqueous solution of common salt, dried over anhydrous potassium carbonate and distilled to remove the solvent. 40 ml of ethanol, 3.2 ml of concentrated hydrochloric acid and 0.3 g of platinum oxide were added to the obtained residue to carry out hydrogenation at a room temperature under 3 kg/cm2 for 6 hours. The catalyst was filtered out and the filtrate was concentrated under a reduced pressure, followed by the addition of concentrated aqueous ammonia. The obtained mixture was extracted with chloroform. The chloroform phase was dried over anhydrous potassium carbonate and distilled to remove the solvent. The residue was purified by silica gel column chromatography [solvent: dichloromethane/methanol/concentrated aqueous ammonia (100:10:1)] to obtain 1.95 g of the title compound as a yellow oil (yield: 55%).

1. customThe obtained mixture was reacted at a room temperature for 16 hours
2. extractionThe obtained mixture was extracted with ethyl acetate
3. washThe ethyl acetate layer was washed with water
4. dry with materiala saturated aqueous solution of common salt, dried over anhydrous potassium carbonate
5. distillationdistilled
6. customto remove the solvent
7. addition40 ml of ethanol, 3.2 ml of concentrated hydrochloric acid and 0.3 g of platinum oxide were added to the obtained residue
8. customat a room temperature
9. customfor 6 hours
10. filtrationThe catalyst was filtered out
11. concentrationthe filtrate was concentrated under a reduced pressure
12. additionfollowed by the addition of concentrated aqueous ammonia
13. extractionThe obtained mixture was extracted with chloroform
14. dry with materialThe chloroform phase was dried over anhydrous potassium carbonate
15. distillationdistilled
16. customto remove the solvent
17. customThe residue was purified by silica gel column chromatography [solvent: dichloromethane/methanol/concentrated aqueous ammonia (100:10:1)]

ORDレコード

ord-0a5ec8defd214c6a8f295007aa708ed7

出典データセット

uspto-grants-1992_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05166188