Sodium Hydroxide → Methyl N-[[[methyl[[(2-methylpropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]amino] carbonyl]oxy]ethanimidothioate

HRID 223443

반응식

HRID 223443 반응식
[CH3:1][N:2]([S:6][N:7]([CH2:18][CH:19]([CH3:21])[CH3:20])[P:8]1(=[S:17])[O:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[O:9]1)[C:3](F)=[O:4].[OH:22][N:23]=[C:24]([S:26][CH3:27])[CH3:25].[OH-].[Na+]>C(Cl)Cl.[Cl-].C([N+](CC)(CC)CC)C.O>[CH3:1][N:2]([S:6][N:7]([CH2:18][CH:19]([CH3:21])[CH3:20])[P:8]1(=[S:17])[O:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[O:9]1)[C:3]([O:22][N:23]=[C:24]([S:26][CH3:27])[CH3:25])=[O:4]

참가 물질

7

반응물 3

HCID 14798Sodium HydroxideHCID 92243Methyl N-hydroxyethanimidothioateHCID 53825165N-methyl[[(2-methylpropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]carbamic fluoride

생성물 1

HCID 54174186Methyl N-[[[methyl[[(2-methylpropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]amino] carbonyl]oxy]ethanimidothioate

시약·촉매·용매 3

HCID 5946Tetraethylammonium Chloride촉매HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

A solution of N-(2-methylpropyl)-2-thioxo-1,3,2-benzodioxaphosphol-2-amine (16.2 g, 66.6 mmol) and triethylamine (7.3 g, 72 mmol) in tetrahydrofuran (50 ml) is added dropwise over 10 minutes to a solution of sulfur dichloride (8.1 g, 78.7 mmol) in tetrahydrofuran (50 ml) with cooling to maintain a temperature of -5° to 0°. After the addition, the mixture is stirred for two hours then diluted with ether (100 ml). The reaction mixture is filtered under nitrogen and the filtrate concentrated in vacuo. The residue is dissolved in dimethyl formamide (50 ml) and N-methyl carbamoyl fluoride (5.8 g, 75.3 mmol) added at once followed by dropwise addition of triethylamine (7.3 g, 72 mmol) in dimethyl formamide (10 ml) over 10 minutes with cooling in a bath at -25°. After the addition the mixture is stirred for two hours in a bath at 0°. The mixture is diluted with ether, washed with ice cold water, dried and concentrated to leave a crude N-methyl[[(2-methylpropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]carbamic fluoride II'''. The carbamic fluoride is dissolved in methylene chloride (50 ml) and a solution of methyl N-hydroxyethanimidothioate (7.00 g, 66.6 mmol), tetraethylammonium chloride (1.00 g, 6.04 mmol) and sodium hydroxide (2.20 g, 80 mmol) in water (50 ml) is added at once. The mixture is stirred for 20 hours at room temperature, the phases separated, and the organic phase washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residual oil is triturated with ether to precipitate the product methyl N-[[[methyl[[(2-methypropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]carbonyl]oxy]ethanimidothioate (I''')

후처리

  1. customthe phases separated
  2. washthe organic phase washed with water
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residual oil is triturated with ether
  6. customto precipitate the product methyl N-[[[methyl[[(2-methypropyl)(2-thioxo-1,3,2-benzodioxaphosphol-2-yl)amino]thio]carbonyl]oxy]ethanimidothioate (I''')

출처 및 근거

ORD 기록
ord-832545dc2f0a420696fcc77d420e0760
출처 데이터셋
uspto-grants-1982_10
특허 번호
US04354975

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