Sodium diethyldithiocarbamate trihydrate → 3-(Benzyloxycarbonylamino)-N-[2-[diethylamino(thiocarbonyl)-thio]ethyl]propionamide

HRID 1583509

반응식

HRID 1583509 반응식
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][C:14]([NH:16][CH2:17][CH2:18]Br)=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.O.O.[CH2:23]([N:25]([CH2:29][CH3:30])[C:26](=[S:28])[S-:27])[CH3:24].[Na+]>CC(C)=O>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][C:14]([NH:16][CH2:17][CH2:18][S:28][C:26]([N:25]([CH2:29][CH3:30])[CH2:23][CH3:24])=[S:27])=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

4

반응물 2

HCID 517546Sodium diethyldithiocarbamate trihydrateHCID 202587523-(benzyloxycarbonylamino)-N-(2-bromoethyl)propionamide

생성물 1

HCID 133361483-(Benzyloxycarbonylamino)-N-[2-[diethylamino(thiocarbonyl)-thio]ethyl]propionamide수율 89.2%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

To the solution of 3-(benzyloxycarbonylamino)-N-(2-bromoethyl)propionamide (10 g) in acetone (250 ml), sodium diethyldithiocarbamate trihydrate (6.8 g) in acetone (150 ml) is added and the mixture is stirred for 40 minutes at room temperature. The reaction mixture is filterd and the filtrate is concentrated in vacuo. The residue is dissolved in ethyl acetate (150 ml) and the solution is washed with N hydrochloric acid, N sodium hydroxide, water and saturated sodium chloride solution in the named order. The ethyl acetate solution is dried over anhydrous magnesium sulfate and concentrated in vacuo to give 10.7 g (89%) of the titled compound.

후처리

  1. concentrationthe filtrate is concentrated in vacuo
  2. dissolutionThe residue is dissolved in ethyl acetate (150 ml)
  3. washthe solution is washed with N hydrochloric acid, N sodium hydroxide, water and saturated sodium chloride solution in the named order
  4. dry with materialThe ethyl acetate solution is dried over anhydrous magnesium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-d85aec25f98640f0976d1ec51fba414a
출처 데이터셋
uspto-grants-1985_11
특허 번호
US04552765

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