Diisopropylethylamine → HCID 67381486, compound
Reaction equation
[NH2:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[CH:5][C:3]=1[NH2:4].[N:10]1([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:17][CH2:16][CH2:15][C@H:11]1[C:12](O)=[O:13].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>CS(C)=O.C(OCC)(=O)C>[NH2:4][C:3]1[CH:5]=[CH:6][C:7]([Br:9])=[CH:8][C:2]=1[NH:1][C:12]([C@@H:11]1[CH2:15][CH2:16][CH2:17][N:10]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[O:13]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of the 2-amino-4-bromoaniline (6.0 g, 32.1 mmol), Boc-Pro-OH (6.90 g, 32.1 mmol) and HATU (13.42 g, 35.3 mmol) in dry DMSO (160 mL) was treated with diisopropylethylamine (14.0 mL, 10.4 g, 80 mmol) followed by stirring at room temperature for 18 h. The mixture was diluted with ethyl acetate and extracted with water (3×) and saturated sodium chloride solution. Drying (Na2SO4) and concentration in vacuo afforded a brown solid which was used directly in the next step.
Workup
- extractionextracted with water (3×) and saturated sodium chloride solution
- customDrying
- concentration(Na2SO4) and concentration in vacuo
- customafforded a brown solid which
Sources & evidence
- ORD record
- ord-e1dfc78fede446a58ef10742dcb1c94f
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006387B2
Reaction notes
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