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Benzoyl chloride → 5-Benzoylamino-2-phenyloxazolo[5,4-b]pyridine

HRID 66366
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반응식

HRID 66366 반응식
[NH2:1][C:2]1[N:7]=[C:6]2[O:8][C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:10][C:5]2=[CH:4][CH:3]=1.[C:17](Cl)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>N1C=CC=CC=1>[C:17]([NH:1][C:2]1[N:7]=[C:6]2[O:8][C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:10][C:5]2=[CH:4][CH:3]=1)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7412Benzoyl chlorideHCID 227547935-Amino-2-phenyloxazolo[5,4-b]pyridine

생성물 1

HCID 227547985-Benzoylamino-2-phenyloxazolo[5,4-b]pyridine

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 80 mg. of 5-amino-2-phenyloxazolo[5,4-b]pyridine in 1 ml. of pyridine was treated with 0.07 ml. of benzoyl chloride. After standing 1 hour the mixture was diluted with ice-water. The precipitate was collected and recrystallized from methanol to give 5-benzoylamino-2-phenyloxazolo[5,4-b]pyridine, m.p. 191°-192° C.

후처리

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The precipitate was collected
  • customrecrystallized from methanol
  • 출처 및 근거

    ORD 기록
    ord-3eade76e1ede47acad219115495f1cd5
    출처 데이터셋
    uspto-grants-1978_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04131677

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