4-Tert-butylbenzene-1,2-diamine → HCID 178496739, compound
Reaction equation
C([NH:8][C@@H:9]([C@@H:13]([O:15][CH3:16])[CH3:14])[C:10](O)=O)(OC(C)(C)C)=O.[C:17]([C:21]1[CH:26]=[CH:25][C:24]([NH2:27])=[C:23]([NH2:28])[CH:22]=1)([CH3:20])([CH3:19])[CH3:18]>>[C:17]([C:21]1[CH:26]=[CH:25][C:24]2[NH:27][C:10]([C@@H:9]([NH2:8])[C@@H:13]([O:15][CH3:16])[CH3:14])=[N:28][C:23]=2[CH:22]=1)([CH3:20])([CH3:18])[CH3:19]Participants
3
Procedure
The title compound was prepared according to Method 4 using N-boc-(2S,3S)-2-amino-3-methoxybutanoic acid and 4-tert-butyl-1,2-diaminobenzene.
Sources & evidence
- ORD record
- ord-d0dc4cca523e414493a9f1abec3a7f49
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927587B2
Reaction notes
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