Hydrazine hydrate (1:1) → 4-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazide

HRID 80964Notes

Reaction equation

HRID 80964 reaction equation
F[B-](F)(F)F.[N:6]1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=[N:7]1.[OH:23][C:24]([CH3:51])([CH3:50])[CH2:25][C@@:26]1([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[O:31][C:30](=[O:32])[N:29]([C@H:33]([C:35]2[CH:43]=[CH:42][C:38]([C:39](O)=[O:40])=[CH:37][CH:36]=2)[CH3:34])[CH2:28][CH2:27]1.C(N(C(C)C)C(C)C)C.O.NN>CN(C)C=O.O>[OH:23][C:24]([CH3:51])([CH3:50])[CH2:25][C@@:26]1([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[O:31][C:30](=[O:32])[N:29]([C@H:33]([C:35]2[CH:43]=[CH:42][C:38]([C:39]([NH:6][NH2:7])=[O:40])=[CH:37][CH:36]=2)[CH3:34])[CH2:28][CH2:27]1

Participants

7

Reactant 4

HCID 24654Hydrazine hydrate (1:1)HCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 581092884-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid

Product 1

HCID 668580744-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazide

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (0.33 g) was added to 4-{(S)-1-[(S)-6-(2-hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid (0.37 g) and EtNiPr2 (0.41 mL) dissolved in N,N-dimethylformamide (5 mL). After stirring the solution at room temperature for 10 min, hydrazine hydrate (0.23 mL) was added. The solution was stirred at room temperature overnight and then diluted with water. The resulting mixture was extracted with ethyl acetate and the combined extracts were washed with brine and dried (MgSO4). The solvent was removed and the residue was purified by chromatography on silica gel (CH2Cl2/MeOH 98:2→90:10) to afford the title compound as a colorless foam-like solid.

Workup

  1. stirringThe solution was stirred at room temperature overnight
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. washthe combined extracts were washed with brine
  4. dry with materialdried (MgSO4)
  5. customThe solvent was removed
  6. customthe residue was purified by chromatography on silica gel (CH2Cl2/MeOH 98:2→90:10)

Sources & evidence

ORD record
ord-388b34173038445495ca16716fd6954b
Source dataset
uspto-grants-2014_09
Patent number
US08846668B2

Reaction notes

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