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Hydrochloric Acid → HCID 9993627, 화합물

HRID 1061846
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인쇄 미리보기

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HRID 1061846 반응식
CO[C:3]1[CH:8]=[CH:7][C:6]([O:9]C)=[CH:5][C:4]=1[NH:11][C:12]([C:14]1[C:23]2[C:18](=[CH:19][C:20]([OH:24])=[CH:21][CH:22]=2)[CH:17]=[CH:16][CH:15]=1)=[O:13].Cl.N1C=CC=CC=1.Cl>>[OH:24][C:20]1[CH:19]=[C:18]2[C:23](=[CH:22][CH:21]=1)[C:14]([C:12]1[O:13][C:3]3[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][C:4]=3[N:11]=1)=[CH:15][CH:16]=[CH:17]2
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참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 10176127Pyridinium chlorideHCID 22285700N-(2,5-Dimethoxyphenyl)-6-hydroxynaphthalene-1-carboxamide

생성물 1

HCID 9993627HCID 9993627, 화합물수율 85%

반응 조건

온도
200 °C

실험 절차

A mixture of N-(2,5-dimethoxyphenyl)-6-hydroxy-1-naphthamide (2.0 g, 6.2 mmol), and pyridine hydrochloride (4.0 g, 34.6 mmol) was heated at 200° C. for 1 h. The reaction mixture was cooled to room temperature, acidified with HCl (2N) and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography (hexanes/EtOAc 1/1) gave a tan solid (1.45 g, 85% yield, m.p. 232-234° C.); MS m/e 278 (M+H)+.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionextracted with EtOAc
  3. dry with materialThe organic extracts were dried over MgSO4
  4. customEvaporation and purification by flash chromatography (hexanes/EtOAc 1/1)

출처 및 근거

ORD 기록
ord-3a9c37bad11a459ea4633126ed94a204
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06960607B2

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