Hydrazine hydrate (1:1) → N-tert-butyl-6-hydrazino-N-methylpyridine-3-sulfonamide
반응식
[C:1]([N:5]([CH3:16])[S:6]([C:9]1[CH:10]=[N:11][C:12](Cl)=[CH:13][CH:14]=1)(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2].O.[NH2:18][NH2:19]>>[C:1]([N:5]([CH3:16])[S:6]([C:9]1[CH:10]=[N:11][C:12]([NH:18][NH2:19])=[CH:13][CH:14]=1)(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2]참가 물질
3
실험 절차
According to the process described in Example 4.2, starting with 0.66 g (2.53 mmol) of N-tert-butyl-6-chloro-N-methylpyridine-3-sulfonamide and 0.46 mL of hydrazine monohydrate, 0.55 g of N-tert-butyl-6-hydrazino-N-methylpyridine-3-sulfonamide is obtained in the form of a white solid, which is used without further purification in the following step.
출처 및 근거
- ORD 기록
- ord-760e306829b447c4a0a47a902c5e1af1
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08697731B2
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