反応式
[Na].[NH2:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][C:4]=1[S:12]([OH:15])(=O)=[O:13].S(Cl)(Cl)(=O)=O.P(Cl)(Cl)(Cl)=O.S1(CCCC1)(=O)=O.[NH3:33]>CO>[NH3:2].[NH2:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][C:4]=1[S:12]([NH2:33])(=[O:15])=[O:13]参加物
9
実験手順
The commercially available sodium salt of 2-amino-5-nitro-benzenesulfonic acid can be converted to the corresponding sulfonyl chloride with phosphoryl chloride in the presence of a suitable co-solvent, such as sulfolane. Treatment with ammonia, e.g., ammonia solution in methanol or ammonia gas, affords the desired 2-amino-5-nitro-benzenesulfonamide intermediate.
出典と根拠
- ORDレコード
- ord-0531f833112e468eaba84e598a136d32
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07582754B2
関連ノート
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