Ammonia → 5-Nitrooxy-pentanoic acid amide

HRID 1625586ノート

反応式

HRID 1625586 の反応式
[N+:1]([O:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]([OH:11])=O)([O-:3])=[O:2].C([N:14](CC)CC)C.ClC(OCC)=O.N.S([O-])([O-])(=O)=O.[Na+].[Na+]>ClCCl>[N+:1]([O:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]([NH2:14])=[O:11])([O-:3])=[O:2]

参加物

7

反応条件

温度
0 °C

実験手順

To a solution of compound 2 (1.30 g, 1.0 eq) in dry dichloromethane (20.0 mL) cooled to 0° C. was added triethylamine (1.30 mL, 1.2 eq) followed by ethyl chloroformate (0.83 mL, 1.1 eq). The reaction mixture was stirred at 0° C. for 45 minutes and 30% aqueous ammonia solution (15.0 mL) was added. The solution was stirred from 0° C. to RT for 18 hours and sodium sulphate was added to dry the mixture. The resulting mixture was filtered off and the filtrate was concentrated under vacuum. The residue was adsorbed on silica gel and purified by flash chromatography [Biotage®, dichloromethane/methanol 100/0→98/2 (120V*), 98/2 (6CV)] affording compound 3 as a white solid (1.10 g, yield=85%).

後処理

  1. stirringThe solution was stirred from 0° C. to RT for 18 hours
  2. customto dry the mixture
  3. filtrationThe resulting mixture was filtered off
  4. concentrationthe filtrate was concentrated under vacuum
  5. custompurified by flash chromatography [Biotage®, dichloromethane/methanol 100/0→98/2 (120V*), 98/2 (6CV)]

出典と根拠

ORDレコード
ord-639aa6d49bbd4e44912f27c282d1a381
出典データセット
uspto-grants-2014_07
特許番号
US08784871B2

反応ノート

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