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Acetic Acid → 5-chloro-1H-pyrrolo(2,3-b)pyridine-3-carbaldehyde

HRID 509966
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HRID 509966 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[CH:10]=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.C1N2CN3CN(C2)CN1C3.[C:21](O)(=[O:23])C>O>[Cl:1][C:2]1[CH:3]=[C:4]2[C:10]([CH:21]=[O:23])=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 4101HexamethylenetetramineHCID 242292135-Chloro-1H-pyrrolo[2,3-b]pyridine

생성물 1

HCID 468564775-chloro-1H-pyrrolo(2,3-b)pyridine-3-carbaldehyde수율 59.2%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

In a round bottom flask, 5-chloro-1H-pyrrolo[2,3-b]pyridine (1, 10.0 g, 65.5 mmol) was combined with hexamethylenetetramine (11.9 g, 85.2 mmol), acetic acid (28.3 mL, 0.498 mol) and 56.7 mL of water. The reaction was heated at reflux overnight, then 200 mL of water was added. After 30 minutes, solid material was collected by filtration and dried to give the desired compound (114, 7.0 g).

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux overnight
  3. filtrationsolid material was collected by filtration
  4. customdried

출처 및 근거

ORD 기록
ord-f4d5c70bb0954c4ba840c615a87a0808
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096593B2

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