Triethylamine → (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid dimethylcarbamoylmethyl ester

HRID 523409Notes

Reaction equation

HRID 523409 reaction equation
Cl[CH2:2][C:3]([N:5]([CH3:7])[CH3:6])=[O:4].[C:8]1([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:13]=[CH:12][C:11]([CH2:14][C@@H:15]([NH:24]C(OC(C)(C)C)=O)[CH2:16][C@:17]([CH2:22][OH:23])([CH3:21])[C:18]([OH:20])=[O:19])=[CH:10][CH:9]=1.CCN(CC)CC>CC(C)=O>[CH3:6][N:5]([CH3:7])[C:3]([CH2:2][O:20][C:18](=[O:19])[C@@:17]([CH2:22][OH:23])([CH3:21])[CH2:16][C@H:15]([NH2:24])[CH2:14][C:11]1[CH:12]=[CH:13][C:8]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[CH:9][CH:10]=1)=[O:4]

Participants

5

Procedure

2-Chloro-N,N-dimethylacetamide (40 μL, 387 μmol) was added to a mixture of (2S,4R)-5-biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-2-methyl-pentanoic acid (100 mg, 242 μmol) and Et3N (35 μL, 254 μmol) in acetone (10 mL). The mixture was refluxed for 24 hours and the reaction monitored for completion. When the reaction was complete, the product was purified ((Interchim reverse phase chromatography column) the solvent was removed under vacuum to yield (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid dimethylcarbamoylmethyl ester.

Workup

  1. temperatureThe mixture was refluxed for 24 hours
  2. customthe product was purified ((Interchim reverse phase chromatography column) the solvent
  3. customwas removed under vacuum

Sources & evidence

ORD record
ord-7951a473e8b44f36b4be40014fd01155
Source dataset
uspto-grants-2016_05
Patent number
US09334245B2

Reaction notes

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