반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH2:12])[C:6]([NH2:13])=[N:5]2.[C:14](OC(=O)CC)(=O)[CH2:15][CH3:16]>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]1[NH:12][C:14]([CH2:15][CH3:16])=[N:13][C:6]1=[N:5]2참가 물질
4
실험 절차
Four parts of 6-chloro-2,3-diaminoquinoxaline was combined with 3 parts of propionic anhydride in 2 parts of tetrahydrofuran. The mixture was heated for three hours during which time a thick slurry formed. The solid was collected from the hot mixture by filtration and washed twice with two parts of tetrahydrofuran. The gray solid was air-dried to give four parts of 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline, m.p. 298°-300°.
후처리
- temperatureThe mixture was heated for three hours during which time a thick slurry
- customformed
- filtrationThe solid was collected from the hot mixture by filtration
- washwashed twice with two parts of tetrahydrofuran
- customThe gray solid was air-dried
출처 및 근거
- ORD 기록
- ord-9e35a6b9f5a54dd29f6ad807ad3dde7b
- 출처 데이터셋
- uspto-grants-1977_05
- 특허 번호
- US04022777
연결된 노트
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