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Boron tribromide → HCID 21706300, 화합물

HRID 1594926
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HRID 1594926 반응식
B(Br)(Br)Br.C[O:6][C:7]1[CH:8]=[C:9]([C:13]2([CH2:21][CH2:22][CH3:23])[O:18][CH2:17][CH2:16][N:15]([CH3:19])[C:14]2=[O:20])[CH:10]=[CH:11][CH:12]=1>C(Cl)Cl>[OH:6][C:7]1[CH:8]=[C:9]([C:13]2([CH2:21][CH2:22][CH3:23])[O:18][CH2:17][CH2:16][N:15]([CH3:19])[C:14]2=[O:20])[CH:10]=[CH:11][CH:12]=1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 21706239HCID 21706239, 화합물

생성물 1

HCID 21706300HCID 21706300, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

BBr3 (1M in CH2Cl2) (0.341 mL, 0.341 mmol) was added dropwise to a solution of 2-(-3-methoxy-phenyl)-4-methyl-2-propyl-morpholine-3-one, as described above in Step D, (0.06 g, 0.227 mmol) in CH2Cl2 (3 mL) at 0° C. with stirring. The ice bath was removed and stirring was continued for 16 h. The reaction mixture was quenched with H2O, concentrated to dryness, then dissolved in MeOH and purified by RP preparative HPLC on a PrepPak (95/5 to 5/95 H2O/CH3CN w/0.1% TFA, flow=65 mL/min) to give the title compound. FAB MS (M+1) 250.

후처리

  1. customThe ice bath was removed
  2. stirringstirring
  3. customThe reaction mixture was quenched with H2O
  4. concentrationconcentrated to dryness
  5. dissolutiondissolved in MeOH
  6. custompurified by RP preparative HPLC on a PrepPak (95/5 to 5/95 H2O/CH3CN w/0.1% TFA, flow=65 mL/min)

출처 및 근거

ORD 기록
ord-c7483fd9aa9a442db5f1101930823c65
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06284755B1

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