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Acetic Acid → 1H-Pyrrolo(2,3-b)pyridine-2-carbaldehyde

HRID 489731
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반응식

HRID 489731 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[CH:3]=[CH:2]1.C1N2CN3CN(C2)CN1C3.[C:20](O)(=[O:22])C>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[CH:3]=[C:2]1[CH:20]=[O:22]
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참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 4101HexamethylenetetramineHCID 92221H-Pyrrolo(2,3-b)pyridine

생성물 1

HCID 218736801H-Pyrrolo(2,3-b)pyridine-2-carbaldehyde수율 58%

실험 절차

To a solution of 7-Azaindole (Aldrich Chemical Co. Cat No. A9,550-2, 4.12 g, 34.9 mmol) in 33% acetic acid (43 ml) was added Hexamethylenetetramine (7.3 g, 5.2 mmol) and the reaction was heated at reflux for 6 hours. The reaction mixture was cooled to room temperature and diluted with ice water (100 ml). The mixture was then left at 0° C. for 18 h. to crystallize product. The beige powder was filtered and washed with water to provide 7-azaindole-2-carboxaldehyde (2.95 g, 58%). 1H NMR (DMSO-d6) δ:7.28 (1H, dd, J=4.8 Hz, 7.9 Hz), 8.37 (1H, dd, J=1.6 Hz, 4.8 Hz), 8.42 (1H, dd, J=1.6 Hz, 7.9 Hz), 8.47 (1H, s), 9.94 (s, 1H).

후처리

  1. temperaturethe reaction was heated
  2. temperatureat reflux for 6 hours
  3. customto crystallize product
  4. filtrationThe beige powder was filtered
  5. washwashed with water

출처 및 근거

ORD 기록
ord-c2592e9705864d8eba7fe25c66918e78
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06979696B2

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