Dimethylformamide → HCID 18617606, 화합물

HRID 1264203노트

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HRID 1264203 반응식
P(Cl)(Cl)([Cl:3])=O.O[CH2:7][CH2:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[CH:12]2.CN([CH:21]=[O:22])C>>[Cl:3][CH2:7][CH2:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[C:12]2[CH:21]=[O:22]

참가 물질

4

반응물 3

HCID 6228Dimethylformamide2회HCID 24813Phosphorus oxychlorideHCID 186174542-(5-indolyl)ethanol

생성물 1

HCID 18617606HCID 18617606, 화합물수율 90%

반응 조건

온도
80 °C

실험 절차

A solution of 1.46 mL (15.7 mmol) phosphorous oxychloride in 5 mL DMF is stirred for 20 minutes. A solution of 2.11 g (13.1 mmol) 5-(2-hydroxyethyl)indole (reference example 6) in 5 mL DMF is added, and the reaction mixture is heated to 80° C. for ten minutes. The reaction is quenched with solid sodium bicarbonate and diluted with 250 mL 1:1 CH2Cl2:MeOH. The inorganic solids are filtered off, and the filtrate concentrated. The resulting residue is refluxed in 75 mL 1N HCl solution for one hour, then extracted with CH2Cl2. The organic extracts are combined and concentrated, and the residue chromatographed (20:1 CH2Cl2:MeOH) to provide 2.45 g of the product as a brown solid in 90% yield. 1H NMR (CDCl3): δ 3.19 (2H, t, J=7 Hz), 3.76 (2H, t, J=7 Hz), 7.20 (1H, dd, J=8, 1 Hz), 7.40 (1H, d, J=8 Hz), 7.85 (1H, d, J=3 Hz), 8.19 (1H, s), 8.98 (1H, br), 10.05 (1H, s). MS (EI) m/z 207, 209 (M[35Cl, 37Cl])+, 158 (M−CH2Cl)+.

후처리

  1. customThe reaction is quenched with solid sodium bicarbonate
  2. additiondiluted with 250 mL 1:1 CH2Cl2
  3. filtrationThe inorganic solids are filtered off
  4. concentrationthe filtrate concentrated
  5. temperatureThe resulting residue is refluxed in 75 mL 1N HCl solution for one hour
  6. extractionextracted with CH2Cl2
  7. concentrationconcentrated
  8. customthe residue chromatographed (20:1 CH2Cl2:MeOH)

출처 및 근거

ORD 기록
ord-aed3470732e144979fb4a2b68379b1a7
출처 데이터셋
uspto-grants-2003_04
특허 번호
US06541505B1

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