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Propargyl bromide → 2-(N-Ethoxycarbonyl-N-propargylaminomethyl)-pyrimidine

HRID 1033752
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반응식

HRID 1033752 반응식
[CH2:1]([O:3][C:4]([NH:6][CH2:7][C:8]1[N:13]=[CH:12][CH:11]=[CH:10][N:9]=1)=[O:5])[CH3:2].[OH-].[K+].[CH2:16](Br)[C:17]#[CH:18]>[Br-].C([N+](CC)(CC)CC1C=CC=CC=1)C.C1(C)C=CC=CC=1>[CH2:1]([O:3][C:4]([N:6]([CH2:7][C:8]1[N:9]=[CH:10][CH:11]=[CH:12][N:13]=1)[CH2:18][C:17]#[CH:16])=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7842Propargyl bromideHCID 14797Potassium HydroxideHCID 189536352-Ethoxycarbonylaminomethyl-pyrimidine

생성물 1

HCID 189536422-(N-Ethoxycarbonyl-N-propargylaminomethyl)-pyrimidine

시약·촉매·용매 2

HCID 165294Benzyltriethylammonium bromide촉매HCID 1140Toluene
용매

실험 절차

18.1 g (0.1 mol) of 2-ethoxycarbonylaminomethyl-pyrimidine are added to a suspension of 20 g (0.3 mol) of pulverized KOH and 1.1 g (5 mmol) of triethylbenzylammoniumbromide in 200 g of toluene, and then 18 g (0.12 mol) of propargylbromide (80% solution in toluene) at room temperature. The mixture is subsequently stirred for 15 hours at room temperature, the salts are filtered off with suction, the filtrate is washed with brine, dried with MgSO4 concentrated and distilled. The reaction product is identical with that of example Z1b.

후처리

  1. customat room temperature
  2. filtrationthe salts are filtered off with suction
  3. washthe filtrate is washed with brine
  4. dry with materialdried with MgSO4
  5. concentrationconcentrated
  6. distillationdistilled

출처 및 근거

ORD 기록
ord-f460d2f9ba3c49f892270fb0fc4022df
출처 데이터셋
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05312823

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