Reaction equation
[CH:1]([C:4]1[C:12]2[S:11][C:10]([NH2:13])=[N:9][C:8]=2[C:7]([CH3:14])=[CH:6][C:5]=1[S:15]C#N)([CH3:3])[CH3:2].SC[C@H]([C@@H](CS)O)O.P([O-])([O-])([O-])=O>CCO>[NH2:13][C:10]1[S:11][C:12]2[C:4]([CH:1]([CH3:2])[CH3:3])=[C:5]([SH:15])[CH:6]=[C:7]([CH3:14])[C:8]=2[N:9]=1Participants
5
Procedure
The title compound was prepared according to General Method 14 using 7-isopropyl-4-methyl-6-thiocyanato-benzothiazol-2-yl-amine (Example L-5; 11.5 g, 43.7 mmol), dithiothreitol (27.0 g, 175 mmol), EtOH (200 mL), and phosphate buffer (50 mL). MS (APCI): 239 (M+H).
Sources & evidence
- ORD record
- ord-d39da9417730475393ffc6d18c387612
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528510B1
Linked notes
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