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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 59323470, 화합물

HRID 2390073
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HRID 2390073 반응식
[CH2:1]([C:3]1[CH:8]=[C:7]([CH2:9][OH:10])[CH:6]=[CH:5][N:4]=1)[CH3:2].C(N(CC)CC)C.[CH3:18][S:19](Cl)(=[O:21])=[O:20]>ClCCl>[CH2:1]([C:3]1[CH:8]=[C:7]([CH2:9][O:10][S:19]([CH3:18])(=[O:21])=[O:20])[CH:6]=[CH:5][N:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 9964106(2-Ethylpyridin-4-yl)methanol

생성물 1

HCID 59323470HCID 59323470, 화합물수율 36.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 82 mg of 2-ethyl-4-hydroxymethylpyridine and 79 mg of triethylamine in dichloromethane (2 mL) was added 82 mg of methanesulfonyl chloride, followed by stirring at room temperature for 1 hour. It was purified by PLC (chloroform:methanol=10:1), dissolved in ethyl acetate, washed with an aqueous sodium bicarbonate solution and then with brine and then dried over anhydrous sodium sulfate, and the solvent was removed by evaporation to obtain 47 mg (yield 36%) of a title compound as a yellow oily substance.

후처리

  1. customIt was purified by PLC (chloroform:methanol=10:1)
  2. dissolutiondissolved in ethyl acetate
  3. washwashed with an aqueous sodium bicarbonate solution
  4. dry with materialwith brine and then dried over anhydrous sodium sulfate
  5. customthe solvent was removed by evaporation

출처 및 근거

ORD 기록
ord-81ec05c99a6548638e25879b11a9efbb
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273766B2

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