反応 #451604

反応方程式

sodium hydroxide

2-(dimethylamino ethyl]-2,3-dihydro-4-phenylmethylpyrido[3,2-f][1,4]oxazepin-5(4H)-one oxalate

dimethylformamide

→

2-[2-(Dimethylamino)ethyl]-2,3-dihydropyrido[3,2-f][1,4]oxazepin-5(4H)-one

溶媒

water

反応条件

後処理

1. 1
   抽出extracted with three 50 ml portions of benzene
2. 2
   抽出The combined benzene extract
3. 3
   乾燥was dried over anhydrous sodium sulfate
4. 4
   濃縮concentrated on the rotary evaporator (steam bath/50 mm)
5. 5
   その他The residue was dried further
6. 6
   その他by azeotroping 2 times with about 50 ml of dry benzene
7. 7
   その他evaporating to dryness each time
8. 8
   workup.DISSOLUTIONThe final residue was dissolved in 40 ml of liquid ammonia and small spheres of sodium
9. 9
   workup.ADDITIONwere added
10. 10
    その他(Addition time was about 1 hr)
11. 11
    workup.ADDITIONThree grams of ammonium chloride was added slowly
12. 12
    その他to evaporate
13. 13
    ろ過the mixture was filtered
14. 14
    濃縮The filtrate was concentrated
15. 15
    その他the residue chromatographed on preparative high pressure liquid chromatograph
16. 16
    洗浄eluting with 75% ethyl acetate/25% dimethylformamide
17. 17
    その他The chemical ionization mass spectrophotometer gave a peak at 236 corresponding to a molecular weight of 235
18. 18
    その他The 1H NMR spectrum of the subject compound was obtained in CDCl3 containing 1% tetramethylsilane (TMS)

実験手順

A solution of 3.0 g (0.006 mole) of 2-[2-(dimethylamino ethyl]-2,3-dihydro-4-phenylmethylpyrido[3,2-f][1,4]oxazepin-5(4H)-one oxalate[1:1.5]-hemihydrate in about 50 ml of water was made basic with dilute aqueous sodium hydroxide solution and then extracted with three 50 ml portions of benzene. The combined benzene extract was dried over anhydrous sodium sulfate and concentrated on the rotary evaporator (steam bath/50 mm). The residue was dried further by azeotroping 2 times with about 50 ml of dry benzene, evaporating to dryness each time. The final residue was dissolved in 40 ml of liquid ammonia and small spheres of sodium were added with stirring to the solution until a blue color persisted for 20 minutes. (Addition time was about 1 hr). Three grams of ammonium chloride was added slowly and the ammonia was allowed to evaporate. The residue was suspended in chloroform and the mixture was filtered. The filtrate was concentrated and the residue chromatographed on preparative high pressure liquid chromatograph using a silica gel column and eluting with 75% ethyl acetate/25% dimethylformamide. The yield of product was 0.1 g (7%). The chemical ionization mass spectrophotometer gave a peak at 236 corresponding to a molecular weight of 235. The 1H NMR spectrum of the subject compound was obtained in CDCl3 containing 1% tetramethylsilane (TMS) and is consistent with the proposed structure and dimethylformamide (DMF) and mineral oil as minor impurities. The chemical shifts, multiplicities, and assignments are given below:

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