3-(Cyclopropylamino)propionitrile → 4-((4-((2-Cyanoethyl)(cyclopropyl)amino)-1-fluorocyclohexyl)methoxy)-3-nitrobenzenesulfonamide

HRID 574954Notes

Reaction equation

HRID 574954 reaction equation
[F:1][C:2]1([CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([S:17]([NH2:20])(=[O:19])=[O:18])=[CH:13][C:12]=2[N+:21]([O-:23])=[O:22])[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.[CH:24]1([NH:27][CH2:28][CH2:29][C:30]#[N:31])[CH2:26][CH2:25]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[C:30]([CH2:29][CH2:28][N:27]([CH:24]1[CH2:26][CH2:25]1)[CH:5]1[CH2:6][CH2:7][C:2]([CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([S:17]([NH2:20])(=[O:19])=[O:18])=[CH:13][C:12]=2[N+:21]([O-:23])=[O:22])([F:1])[CH2:3][CH2:4]1)#[N:31]

Participants

5

Procedure

To a solution of EXAMPLE 363B (200 mg) in dichloromethane (6 mL) was added 3-(cyclopropylamino)propanenitrile (64 mg) followed by sodium triacetoxyborohydride (184 mg). The mixture was stirred overnight. The reaction mixture was diluted with dichloromethane (400 mL) and washed with 2N aqueous NaOH, water, and brine. After drying over Na2SO4, the mixture was filtered and evaporation of the solvent gave the title compound.

Workup

  1. washwashed with 2N aqueous NaOH, water, and brine
  2. dry with materialAfter drying over Na2SO4
  3. filtrationthe mixture was filtered
  4. customevaporation of the solvent

Sources & evidence

ORD record
ord-6b35179adb02433eac74f82766f6c806
Source dataset
uspto-grants-2015_05
Patent number
US09034875B2

Reaction notes

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