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Acetic Acid → 6-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde

HRID 1749807
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인쇄 미리보기

반응식

HRID 1749807 반응식
[Br:1][C:2]1[N:7]=[C:6]2[NH:8][CH:9]=[CH:10][C:5]2=[CH:4][CH:3]=1.[C:11](O)(=[O:13])C.C1N2CN3CN(C2)CN1C3>O>[Br:1][C:2]1[N:7]=[C:6]2[NH:8][CH:9]=[C:10]([CH:11]=[O:13])[C:5]2=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 4101HexamethylenetetramineHCID 111599156-Bromo-7-azaindole

생성물 1

HCID 184006656-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde수율 25%

시약·촉매·용매 1

HCID 962Water용매2회

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온도
120 °C

실험 절차

6-Bromo-1H-pyrrolo[2,3-b]pyridine (0.028 g, 0.14 mmol) was successively added with acetic acid (0.1 mL), water (0.2 mL), and hexamethylenetetramine (0.028 g, 0.20 mmol), and then the mixture was stirred overnight at 120° C. in a sealed tube. The reaction mixture was added with water, and the precipitated solid was collected by filtration to obtain 6-bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde (0.008 g, 25%).

후처리

  1. filtrationthe precipitated solid was collected by filtration

출처 및 근거

ORD 기록
ord-54e04f4ed5f144b7826a660df3b6b91a
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156827B2

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