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Water → HCID 86728277, 화합물

HRID 1776886
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HRID 1776886 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:19]C)=[C:6]([C:8]2[N:9]=[C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][N:11]3[C:16]=2[CH:17]=[O:18])[CH:7]=1.B(Br)(Br)Br.O>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:19])=[C:6]([C:8]2[N:9]=[C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][N:11]3[C:16]=2[CH:17]=[O:18])[CH:7]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 86728276HCID 86728276, 화합물

생성물 1

HCID 86728277HCID 86728277, 화합물수율 48%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
25 °C

실험 절차

2-(5-bromo-2-methoxyphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (0.1 g, 3 mmol) was dissolved in dichloromethane (0.5 mL) at −78° C. BBr3 (1 mL) was added by dropwise stirred for 2 hours at that temperature. Then warmed to 25° C. and stirred for 10 hours. H2O (20 mL) was added by dropwise at −78° C. and extracted with EtOAc (3*50 mL), washed by aq NaHCO3 (3*50 mL) and brine (50 mL). After concentrated, the resulting residue was purified using Prep-TLC (petroleum ether:EtOAc=3:1) to provide 2-(5-bromo-2-hydroxyphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (40 mg, yield: 48%). 1H-NMR (CDCl3, 400 MHz) δ 10.29 (s, 1H), 9.76 (s, 1H), 7.78˜7.79 (m, 2H), 7.65˜7.69 (m, 1H), 7.46˜7.48 (m, 1H), 7.20˜7.22 (m, 1H), 7.00˜7.02 (m, 1H). MS (M+H)+: 317/319.

후처리

  1. stirringstirred for 10 hours
  2. extractionextracted with EtOAc (3*50 mL)
  3. washwashed by aq NaHCO3 (3*50 mL) and brine (50 mL)
  4. concentrationAfter concentrated
  5. customthe resulting residue was purified

출처 및 근거

ORD 기록
ord-0bc6fab644f24d7d8d7d4098a7f16542
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09265773B2

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