반응식
N(C1C(C(OCC)=O)=CN=C2N(CC3OC=CC=3)N=CC=12)N.C(N1C2=NC=C(C(OCC)=O)C(NN)=C2C=N1)C.[CH2:41]([N:47]1[C:51]2[N:52]=[CH:53][C:54]3[C:55](=[O:63])[NH:56][C:57]4[N:58]([N:60]=[CH:61][N:62]=4)[C:59]=3[C:50]=2[CH:49]=[N:48]1)[C:42]1[O:46][CH:45]=[CH:44][CH:43]=1.[C:64]1(O)[CH:69]=[CH:68][CH:67]=[CH:66][CH:65]=1>C(O)C>[CH2:41]([N:47]1[C:51]2[N:52]=[CH:53][C:54]3[C:55]([O:63][C:64]4[CH:69]=[CH:68][CH:67]=[CH:66][CH:65]=4)=[N:56][C:57]4[N:58]([N:60]=[CH:61][N:62]=4)[C:59]=3[C:50]=2[CH:49]=[N:48]1)[C:42]1[O:46][CH:45]=[CH:44][CH:43]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
By substituting 4-hydrazino-1-furfurylpyrazolo-[3,4-b]pyridine-5-carboxylic acid, ethyl ester for the 1-ethyl-4-hydrazino-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester in Example 1 a, 8-furfuryl-4H-pyrazolo-[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidin-5(8H)-one is obtained. This compound is now processed as in Example 1 b and then as in Example 4, substituting phenol for the ethanol to obtain 8-furfuryl-5-phenyloxy-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo-[1,5-a]pyrimidine.
후처리
- customis obtained
출처 및 근거
- ORD 기록
- ord-116dd96379cd429e8faee956d7404e63
- 출처 데이터셋
- uspto-grants-1978_11
- 특허 번호
- US04127655
연결된 노트
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