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Azepan-4-ol → Methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate

HRID 1754300
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HRID 1754300 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[S:12](Cl)(=[O:14])=[O:13].[NH:16]1[CH2:22][CH2:21][CH2:20][CH:19]([OH:23])[CH2:18][CH2:17]1>C(Cl)Cl>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[S:12]([N:16]1[CH2:22][CH2:21][CH2:20][CH:19]([OH:23])[CH2:18][CH2:17]1)(=[O:14])=[O:13]
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참가 물질

4

반응물 2

HCID 5149746Azepan-4-olHCID 194291974-Bromo-3-chlorosulfonyl-benzoic acid methyl ester

생성물 1

HCID 118222058Methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate수율 77.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
25 °C

실험 절차

To a solution of methyl 4-bromo-3-chlorosulfonyl-benzoate (7.22 g, 23.03 mmol, 1.00 Eq) in DCM (100 mL) was added azepan-4-ol (2.65 g, 23.03 mmol, 1.00 Eq) and TEA (2.33 g, 23.03 mmol, 1.00 Eq). The resulting mixture was stirred at 25° C. until the starting material was consumed. The solvent was removed and the residue was purified by silica gel chromatography (PE:EA=1:1) to give desired compound methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate (7.00 g, 17.85 mmol, 77.49% yield). LCMS: 393/395 [M+1].

후처리

  1. customwas consumed
  2. customThe solvent was removed
  3. customthe residue was purified by silica gel chromatography (PE:EA=1:1)

출처 및 근거

ORD 기록
ord-131c3ad461b842a69d21fcb47ddda90b
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169212B2

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