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Methyl iodide → HCID 68564892, 화합물

HRID 2061031
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HRID 2061031 반응식
[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][N:5]([CH3:23])[C:6](=[O:22])[CH2:7][C:8]([NH:11][C:12](=[O:21])[O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)([CH3:10])[CH3:9].[CH3:25][I:26]>C(O)C>[I-:26].[CH2:14]([O:13][C:12]([NH:11][C:8]([CH3:10])([CH3:9])[CH2:7][C:6]([N:5]([CH2:4][CH2:3][N+:2]([CH3:25])([CH3:1])[CH3:24])[CH3:23])=[O:22])=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 60134427HCID 60134427, 화합물

생성물 1

HCID 68564892HCID 68564892, 화합물수율 74%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
50 °C

실험 절차

Benzyl 4-((2-(dimethylamino)ethyl)(methyl)amino)-2-methyl-4-oxobutan-2-ylcarbamate (2.08 g, 6.2 mmol) was dissolved in a solution of ethanol (4 ml) and methyl iodide (30 ml). The mixture was stirred at 50° C. for 18 hours. The reaction mixture was concentrated in vacuo and dissolved in water. The aqueous mixture was washed with ethyl acetate. The washed aqueous mixture concentrated in vacuo to give 2.19 g (74%) of 2-(3-(benzyloxycarbonylamino)-N,3-dimethylbutanamido)-N,N,N-trimethylethanaminium iodide. MS (ESI+) calculated for C19H32N3O3+: 350.24, Found: 350.2 (M+).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutiondissolved in water
  3. washThe aqueous mixture was washed with ethyl acetate
  4. concentrationThe washed aqueous mixture concentrated in vacuo

출처 및 근거

ORD 기록
ord-f8b45931b3e04a869b48a5c05c633be2
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278482B2

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