Acetic Acid Mixture with Hydrobromic Acid → (S)-3-amino-1-((1S,2R,4R)-4-(isopropyl(methyl)amino)-2-(ethylsulfonylmethyl)cyclohexyl)pyrrolidin-2-one

HRID 1374342Notes

Reaction equation

HRID 1374342 reaction equation
[CH:1]([N:4]([CH3:34])[C@@H:5]1[CH2:10][CH2:9][C@H:8]([N:11]2[CH2:15][CH2:14][C@H:13]([NH:16]C(=O)OCC3C=CC=CC=3)[C:12]2=[O:27])[C@H:7]([CH2:28][S:29]([CH2:32][CH3:33])(=[O:31])=[O:30])[CH2:6]1)([CH3:3])[CH3:2].Br.CC(O)=O>CCOCC>[NH2:16][C@H:13]1[CH2:14][CH2:15][N:11]([C@H:8]2[CH2:9][CH2:10][C@@H:5]([N:4]([CH:1]([CH3:3])[CH3:2])[CH3:34])[CH2:6][C@H:7]2[CH2:28][S:29]([CH2:32][CH3:33])(=[O:31])=[O:30])[C:12]1=[O:27]

Participants

4

Reactant 2

HCID 21893785Acetic Acid Mixture with Hydrobromic AcidHCID 86596895HCID 86596895, compound

Product 1

HCID 68767729(S)-3-amino-1-((1S,2R,4R)-4-(isopropyl(methyl)amino)-2-(ethylsulfonylmethyl)cyclohexyl)pyrrolidin-2-oneYield 82.4%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

The entirety of benzyl (S)-1-((1S,2R,4R)-4-(isopropyl(methyl)amino)-2-(ethylsulfonylmethyl)cyclohexyl)-2-oxopyrrolidin-3-ylcarbamate prepared in Step 2 (250 mg) was charged with 30% HBr/AcOH (5 mL). The reaction vessel warms and a vigorous gas evolution occurs. The mixture was stirred for 25 min at RT and then the flask was placed in a cool water bath before the addition of 20 mL of Et2O. The resulting solid was collected, washed with Et2O twice, and concentrated in vacuo to give (S)-3-amino-1-((1S,2R,4R)-4-(isopropyl(methyl)amino)-2-(ethylsulfonylmethyl)cyclohexyl)pyrrolidin-2-one (150 mg). MS found: (M+H)+=360.

Workup

  1. customThe resulting solid was collected
  2. washwashed with Et2O twice
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-2bbd3a4a7b444cedba4899be840b0d3e
Source dataset
uspto-grants-2007_01
Patent number
US07163937B2

Reaction notes

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