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Triethyl orthoacetate → 6-bromo-2,3-dimethyl-3H-imidazo[4,5-b]pyridine

HRID 879542
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HRID 879542 반응식
[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH:8][CH3:9])=[N:6][CH:7]=1.CC(O[CH2:20][CH3:21])(OCC)OCC>CC(O)=O>[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:20]([CH3:21])[N:8]([CH3:9])[C:5]2=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 66221Triethyl orthoacetateHCID 151940325-Bromo-N2-methylpyridine-2,3-diamine

생성물 1

HCID 121829336-bromo-2,3-dimethyl-3H-imidazo[4,5-b]pyridine

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
80 °C

실험 절차

To a suspension of 5-bromo-N2-methylpyridine-2,3-diamine (510 mg, 2.51 mmol) in AcOH (20 mL) was added MeC(OEt)3 (1 mL) and the solution was warmed to 80° C. for 2 hours. The reaction mixture was allowed to cool to room temperature and was concentrated in vacuo. The crude residue was purified by silica gel column chromatography (0-25% THF/CH2Cl2 gradient) to afford the desired product. 1H NMR (400 MHz, CDCl3) δ 8.36 (d, J=1.8 Hz, 1H), 8.06 (d, J=1.9 Hz, 1H), 3.80 (s, 3H), 2.65 (s, 3H).

후처리

  1. temperatureto cool to room temperature
  2. concentrationwas concentrated in vacuo
  3. customThe crude residue was purified by silica gel column chromatography (0-25% THF/CH2Cl2 gradient)

출처 및 근거

ORD 기록
ord-7171941344074b899a7173a9c0b84513
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08987250B2

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