Dimethyl Sulfoxide → HCID 22047043, 화합물

HRID 1073001노트

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HRID 1073001 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Br:11][C:12]1[C:20]2[C:15](=[CH:16][N:17]=[C:18]([CH2:21][OH:22])[CH:19]=2)[O:14][CH:13]=1.CCN(CC)CC>C1COCC1.C(Cl)Cl>[Br:11][C:12]1[C:20]2[C:15](=[CH:16][N:17]=[C:18]([CH:21]=[O:22])[CH:19]=2)[O:14][CH:13]=1

참가 물질

7

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온도
-78 °C

실험 절차

Oxalyl chloride (1.77 mL, 20.1 mmol) is combined with CH2Cl2 (60 mL) in a dried flask under nitrogen, cooled to −78° C., treated dropwise with DMSO (2.86 mL, 40.25 mmol) and stirred for 20 min. The cooled solution is treated drop-wise with a solution of (3-bromofuro[2,3-c]pyridin-5-yl)methanol (4.0 mg, 17.5 mmol) in THF (50 mL), stirred for 1 h, then treated drop-wise with Et3N (12.2 mL, 87.5 mmol). The mixture is stirred for 30 min at −78° C., then 30 min at 0° C. The mixture is washed with saturated NaHCO3 (120 mL) and the organics dried over K2CO3 and concentrated in vacuo to a dark yellow solid (3.91 g). The crude material is chromatographed over 150 g slurry-packed silica gel, eluting with 30% EtOAc/hexane. The appropriate fractions are combined and concentrated in vacuo to afford 3.93 g (99%) of 3-bromofuro[2,3-c]pyridine-5-carbaldehyde as a white solid. MS (EI) m/z: 225 (M+).

후처리

  1. stirringstirred for 1 h
  2. stirringThe mixture is stirred for 30 min at −78° C.
  3. custom30 min
  4. customat 0° C
  5. washThe mixture is washed with saturated NaHCO3 (120 mL)
  6. dry with materialthe organics dried over K2CO3
  7. concentrationconcentrated in vacuo to a dark yellow solid (3.91 g)
  8. customThe crude material is chromatographed over 150 g slurry-packed silica gel
  9. washeluting with 30% EtOAc/hexane
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9c1f3543e4fe48409cb1416fec9ddc31
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06911543B2

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