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Water → HCID 131734966, 화합물

HRID 922471
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HRID 922471 반응식
COCCC[N:6]1[C:14]2[CH:13]=[C:12]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:11]=[CH:10][C:9]=2[CH:8]=[CH:7]1.BrN1C(=O)CC[C:22]1=[O:27].O.Cl[CH2:30]Cl>>[CH3:30][O:27][CH2:22][CH2:19][CH2:18][O:17][C:15]([C:12]1[N:11]=[CH:10][C:9]2[CH:8]=[CH:7][NH:6][C:14]=2[CH:13]=1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 962WaterHCID 6344DichloromethaneHCID 67184N-bromobutanimideHCID 89925499HCID 89925499, 화합물

생성물 1

HCID 131734966HCID 131734966, 화합물

실험 절차

To a solution of ethyl 1-(3-methoxypropyl)-1H-pyrrolo[3,2-c]pyridine-6-carboxylate (2.00 g) in dichloromethane (40 mL) was added N-bromosuccinimide (1.49 g) under ice-cooling, and the mixture was stirred at room temperature for 3 hours. To the reaction solution was added water, and the mixture was extracted with chloroform. The organic layer was washed with saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1→4/1) to give ethyl 3-bromo-1-(3-methoxypropyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylate [REx(105-3)] (2.12 g) as a yellow oil.

후처리

  1. temperaturecooling
  2. extractionthe mixture was extracted with chloroform
  3. washThe organic layer was washed with saturated saline
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe resulting residue was purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1→4/1)

출처 및 근거

ORD 기록
ord-96570c1f7b1e441599b54b641b4c6591
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278944B2

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