Water → HCID 66645054, compound

HRID 2061687Notes

Reaction equation

HRID 2061687 reaction equation
I(C1C=CC=CC=1C(O)=O)(=O)=O.[CH2:13]([N:20]([C:50]([O:52][C:53]([CH3:56])([CH3:55])[CH3:54])=[O:51])[NH:21][C:22](=[O:49])[CH:23]([OH:48])[CH:24]([NH:32][C:33]([C@H:35]1[CH2:39][CH2:38][C:37](=[O:40])[N:36]1[CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)=[O:34])[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C([O-])(O)=O.[Na+].O>CS(C)=O>[CH2:13]([N:20]([C:50]([O:52][C:53]([CH3:56])([CH3:55])[CH3:54])=[O:51])[NH:21][C:22](=[O:49])[C:23](=[O:48])[CH:24]([NH:32][C:33]([C@H:35]1[CH2:39][CH2:38][C:37](=[O:40])[N:36]1[CH2:41][C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1)=[O:34])[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

6

Procedure

IBX (189 mg, 0.303 mmol, 45 wt %) was added a solution of tert-butyl 1-benzyl-2-(3-((R)-1-benzyl-5-oxopyrrolidine-2-carboxamido)-2-hydroxy-4-phenylbutanoyl)-hydrazinecarboxylate (130 mg, 0.216 mmol) in DMSO (3 mL). After stirring overnight saturated aqueous NaHCO3 solution (15 mL) and water (15 mL) were added. The mixture was extracted with EtOAc, the combined organic layers were washed with saturated aqueous NaHCO3 solution, water and dried (MgSO4). Purification by flash column chromatography (gradient 1-10% MeOH in DCM) provided the title compound (110 mg, 85%).

Workup

  1. additionwere added
  2. extractionThe mixture was extracted with EtOAc
  3. washthe combined organic layers were washed with saturated aqueous NaHCO3 solution, water
  4. dry with materialdried (MgSO4)
  5. customPurification by flash column chromatography (gradient 1-10% MeOH in DCM)

Sources & evidence

ORD record
ord-fc23ab95d9854217b0552116aee8ee39
Source dataset
uspto-grants-2012_10
Patent number
US08283363B2

Reaction notes

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