Methylamine → HCID 22217724, compound
Reaction equation
[C:1]([NH:4][C:5]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:6]=1[CH:7]=[CH:8][CH:9]=[C:10]2[S:15](Cl)(=[O:17])=[O:16])(=[O:3])[CH3:2].[CH3:19][NH2:20]>C(O)C>[CH3:19][NH:20][S:15]([C:10]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:11]=1[CH:12]=[CH:13][CH:14]=[C:5]2[NH:4][C:1](=[O:3])[CH3:2])(=[O:17])=[O:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.10 g of 5-acetylaminonaphthalene-1-sulfonyl chloride is dissolved in 8 mL of ethanol and 8 mL of methylamine solution in ethanol are added dropwise. Then the resulting mixture is stirred at reflux temperature for 3.5 hours and the solvent is distilled off in vacuo. The residue is purified by chromatography. Yield: 0.50 g.
Workup
- temperatureat reflux temperature for 3.5 hours
- distillationthe solvent is distilled off in vacuo
- customThe residue is purified by chromatography
Sources & evidence
- ORD record
- ord-c1313fc8d512488a9ada1cbece861b4f
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07026475B2
Reaction notes
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