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Triethylamine → 4-(Chloromethyl)-6-methoxy-quinoline

HRID 1169661
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HRID 1169661 반응식
C(N(CC)CC)C.CS([Cl:12])(=O)=O.O[CH2:14][C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([O:25][CH3:26])[CH:23]=2)[N:18]=[CH:17][CH:16]=1>ClCCl>[Cl:12][CH2:14][C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([O:25][CH3:26])[CH:23]=2)[N:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 3385004-Hydroxymethyl-6-methoxyquinoline

생성물 1

HCID 179006174-(Chloromethyl)-6-methoxy-quinoline

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1.16 ml of triethylamine and 0.64 ml of methanesulfonyl chloride are successively added to a solution of 1.2 g of 4-hydroxymethyl-6-methoxyquinoline in 45 ml of dichloromethane, under an inert atmosphere of argon at a temperature in the region of 20° C. Stirring is maintained at this temperature for 3 hours. The reaction medium is concentrated under reduced pressure to give a brown residue. The product is used without further purification in the following step.

후처리

  1. temperatureis maintained at this temperature for 3 hours
  2. concentrationThe reaction medium is concentrated under reduced pressure
  3. customto give a brown residue
  4. customThe product is used without further purification in the following step

출처 및 근거

ORD 기록
ord-ced5b089534a40448ec45cadf4477ff0
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07825115B2

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