Diisopropylethylamine → HCID 67381486, compound

HRID 1470954Notes

Reaction equation

HRID 1470954 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

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

  1. extractionextracted with water (3×) and saturated sodium chloride solution
  2. customDrying
  3. concentration(Na2SO4) and concentration in vacuo
  4. 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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