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N-Bromosuccinamide → HCID 117728336, 화합물

HRID 1772659
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HRID 1772659 반응식
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[O:11][CH2:12][C:13]1[N:14]=[C:15]2[C:20]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)=[N:19][CH:18]=[CH:17][N:16]2[CH:27]=1.[Br:28]NC(=O)CCC(N)=O>C(Cl)Cl>[Br:28][C:17]1[N:16]2[CH:27]=[C:13]([CH2:12][O:11][C:2]3[CH:3]=[CH:4][C:5]4[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=4)[N:1]=3)[N:14]=[C:15]2[C:20]([N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)=[N:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9834204N-BromosuccinamideHCID 1177283094-(2-((Quinolin-2-yloxy)methyl)imidazo[1,2-a]pyrazin-8-yl)morpholine

생성물 1

HCID 117728336HCID 117728336, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A mixture of compound 31a (5.0 g, 14 mmol) and N-bromosuccinamide (2.5 g, 14 mmol) in DCM (300 mL) at 0° C. was allowed to stir at rt for 10 min. The reaction mixture was diluted with DCM (600 mL) and washed with saturated NaHCO3 (500 mL) and brine (500 mL). The DCM layer was separated, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue obtained was triturated with EtOAc to give compound 31b as a white solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C20H18BrN5O2: 440.1 (M+H). found: 440.0.

후처리

  1. washwashed with saturated NaHCO3 (500 mL) and brine (500 mL)
  2. customThe DCM layer was separated
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe residue obtained
  7. customwas triturated with EtOAc

출처 및 근거

ORD 기록
ord-35cc242a72f34dd89640cbe161074c10
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249163B2

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