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2-Aminopyridine → HCID 22497154, 화합물

HRID 1816020
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HRID 1816020 반응식
[Cl:1][CH:2]1[CH:12]=[CH:11][CH:5]2[C:6]([O:8][C:9](=[O:10])[CH:4]2[CH2:3]1)=O.[NH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1>>[N:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[N:13]1[C:9](=[O:10])[CH:4]2[CH2:3][CH:2]([Cl:1])[CH:12]=[CH:11][CH:5]2[C:6]1=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 104392-AminopyridineHCID 54187688HCID 54187688, 화합물

생성물 1

HCID 22497154HCID 22497154, 화합물수율 97%

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온도
130 °C

실험 절차

119.5 grams (0.64 moles) of 4-chlorotetrahydrophthalic anhydride and 94.1 grams (0.64 moles) of 2-aminopyridine were added to a 500-mL, 3-necked, round-bottomed flask equipped with a Dean-Stark trap topped with a condenser, a nitrogen outlet, means for maintaining a mild sweep of nitrogen over the reaction mixture, and a magnetic stir. The material was heated to 130° C. with an externally heated oil bath to provide an easily stirred melt. The reaction was heated to 175° C. for a 45 minute period. The water of imidization collected in the Dean-Stark trap. The reaction was then heated to 220 to 225° C. for 2.5 hours and the resulting amber material was transferred into a clean glass jar. The crude material was recovered in 97% yield. HPLC analysis of the crude material indicated >98% purity of the desired compound.

후처리

  1. custom3-necked, round-bottomed flask equipped with a Dean-Stark trap
  2. customtopped with a condenser, a nitrogen outlet
  3. temperaturefor maintaining a mild sweep of nitrogen over the reaction mixture
  4. customto provide
  5. temperatureThe reaction was heated to 175° C. for a 45 minute period
  6. customThe water of imidization collected in the Dean-Stark trap
  7. temperatureThe reaction was then heated to 220 to 225° C. for 2.5 hours
  8. customThe crude material was recovered in 97% yield

출처 및 근거

ORD 기록
ord-d24aff7fabad4e76a4a485272adf53f2
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06881815B2

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