4-Tert-butylbenzene-1,2-diamine → HCID 178462344, compound

HRID 1424193Notes

Reaction equation

HRID 1424193 reaction equation
[C:1]([NH:8][C@H:9]([C:13](O)=O)[C@@H:10]([CH3:12])[OH:11])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:16]([C:20]1[CH:25]=[CH:24][C:23]([NH2:26])=[C:22]([NH2:27])[CH:21]=1)([CH3:19])([CH3:18])[CH3:17]>>[C:16]([C:20]1[CH:25]=[CH:24][C:23]2[NH:26][C:13]([C@@H:9]([NH:8][C:1](=[O:2])[O:3][C:4]([CH3:5])([CH3:6])[CH3:7])[C@H:10]([OH:11])[CH3:12])=[N:27][C:22]=2[CH:21]=1)([CH3:19])([CH3:17])[CH3:18]

Participants

3

Reactant 2

HCID 4327084-Tert-butylbenzene-1,2-diamineHCID 2724766N-tert-Butoxycarbonyl-L-threonine

Product 1

HCID 178462344HCID 178462344, compound

Procedure

The title compound was prepared according to Method 4 Steps 1 and 2 using N-Boc-L-threonine (Preparation 52) and 4-tert-butyl-diaminobenzene.

Sources & evidence

ORD record
ord-04afbfbe3b134a2a8d15907fea6e4f83
Source dataset
uspto-grants-2015_01
Patent number
US08927587B2

Reaction notes

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