Diisopropylethylamine → HCID 67775752, compound

HRID 84843Notes

Reaction equation

HRID 84843 reaction equation
[Br:1][C:2]1[CH:9]=[C:8](F)[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[NH2:11][CH2:12][C@@H:13]([NH:17][C:18](=[O:24])[O:19][C:20]([CH3:23])([CH3:22])[CH3:21])[CH2:14][O:15][CH3:16].CCN(C(C)C)C(C)C>CS(C)=O.CCOC(C)=O>[Br:1][C:2]1[CH:9]=[C:8]([NH:11][CH2:12][C@@H:13]([NH:17][C:18](=[O:24])[O:19][C:20]([CH3:22])([CH3:21])[CH3:23])[CH2:14][O:15][CH3:16])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]

Participants

6

Reactant 3

HCID 81531DiisopropylethylamineHCID 1189392-Bromo-4-fluorobenzonitrileHCID 59199768tert-butyl N-((2R)-1-amino-3-methoxypropan-2-yl)carbamate

Product 1

HCID 67775752HCID 67775752, compoundYield 78.1%

Reagents, catalysts & solvents 2

HCID 679Dimethyl SulfoxideSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
100 °C

Procedure

To a solution of 2-bromo-4-fluorobenzonitrile (0.2 g, 1 mmol) in DMSO (3 mL) was added (R)-tert-butyl 1-amino-3-methoxypropan-2-ylcarbamate (0.22 g, 1.08 mmol) and DIPEA (0.267 mL, 1.5 mmol). The mixture was heated at 100° C. for 15 h, and was diluted with EtOAc and washed with 1N HCl and Sat. NaHCO3. The organic phase was separated, dried over Na2SO4, concentrated in vacuo to give (R)-tert-butyl 1-(3-bromo-4-cyanophenylamino)-3-methoxypropan-2-ylcarbamate (0.3 g).

Workup

  1. washwashed with 1N HCl and Sat. NaHCO3
  2. customThe organic phase was separated
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5a25b2abd4604e2d9bad68ab2fc3a528
Source dataset
uspto-grants-2014_09
Patent number
US08846928B2

Reaction notes

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