Triethylamine → HCID 131717757, compound
Reaction equation
Cl.[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N:9]1[C:13](=[O:14])[C:12]2[CH:15]=[C:16]([N+]([O-])=O)[CH:17]=[CH:18][C:11]=2[S:10]1.C(N(CC)CC)C.[CH3:29][O:30][CH:31]=[CH2:32].[CH:33]1[C:38](=[O:39])[O:37][C:35](=[O:36])[CH:34]=1>CN(C=O)C.O>[CH3:29][O:30][CH:31]=[CH2:32].[CH:33]1[C:38](=[O:39])[O:37][C:35](=[O:36])[CH:34]=1.[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N:9]1[C:13](=[O:14])[C:12]2[CH:15]=[CH:16][CH:17]=[CH:18][C:11]=2[S:10]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1.0 g (3 mmol) of the above synthesized N-(6-aminohexyl)-5-nitrobenzoisothiazol-3-one hydrochloride in 25 mL of was prepared and 0.83 mL (5.9 mmol) of triethylamine added. This was added dropwise to a mixture of 0.89 g (6 mmol of anhydride) of Gantrez AN 119 (M.W. 20,000, GAF Corp.) in 15 mL of DMF. After stirring for 30 min, another 0.41 mL (3 mmol) of triethylamine in 45 mL of H2O was added and the mixture stirred for 30 min.
Workup
- customof was prepared
- stirringthe mixture stirred for 30 min.
Sources & evidence
- ORD record
- ord-cda3a6d6ea014965bcba2743a35e6cfe
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05187265
Reaction notes
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