Hydrochloric Acid → Toluene-4-thiosulfonic acid S-(4,5-diamino-2-tert-butyl-phenyl) Ester
Reaction equation
C(OC([NH:8][C:9]1[C:14]([NH:15]C(OC(C)(C)C)=O)=[CH:13][C:12]([S:23][S:24]([C:27]2[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=2)(=[O:26])=[O:25])=[C:11]([C:34]([CH3:37])([CH3:36])[CH3:35])[CH:10]=1)=O)(C)(C)C.Cl>C(Cl)Cl>[NH2:8][C:9]1[C:14]([NH2:15])=[CH:13][C:12]([S:23][S:24]([C:27]2[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=2)(=[O:26])=[O:25])=[C:11]([C:34]([CH3:37])([CH3:36])[CH3:35])[CH:10]=1Participants
4
Procedure
The title compound was prepared as described in Example VV-1 from toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl)ester (prepared in Example UU-2; 15 g, 28 mmol), CH2Cl2 (100 mL), and HCl gas. MS(APCI): 351 (M+H).
Sources & evidence
- ORD record
- ord-3d976d0590c74beea9760d1b8cc11b3b
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06852711B2
Reaction notes
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