Triphenylphosphine → HCID 86731249, compound

HRID 2277190Notes

Reaction equation

HRID 2277190 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[O:16][C:17]3[C:23]([F:24])=[C:22]([OH:25])[CH:21]=[CH:20][C:18]=3[N:19]=2)=[CH:11][C:10]=1[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[CH2:28][C@@H:29]([NH:31][C:32](=[O:38])OC(C)(C)C)[CH3:30].[C:39]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(C)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.Cl.C(OCC)(=O)C>C1COCC1>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[O:16][C:17]3[C:23]([F:24])=[C:22]([O:25][CH2:28][C@@H:29]([NH:31][C:32](=[O:38])[CH3:39])[CH3:30])[CH:21]=[CH:20][C:18]=3[N:19]=2)=[CH:11][C:10]=1[F:26])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

7

Reactant 5

HCID 11776TriphenylphosphineHCID 70231031,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 21866389Hydrogen chloride-ethyl acetateHCID 66880968DIAD tolueneHCID 86731250HCID 86731250, compound

Product 1

HCID 86731249HCID 86731249, compoundYield 74.6%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 2-(4-(benzyloxy)-3-fluorophenyl)-7-fluoro-1,3-benzoxazol-6-ol (1.13 g), tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate (0.841 g) and triphenylphosphine (1.26 g) in THF (20 mL) was added dropwise diisopropyl azodicarboxylate toluene solution (1.9 M, 2.52 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give a white solid. To the obtained solid was added 4 M hydrogen chloride/ethyl acetate (10 mL), and the mixture was stirred at room temperature for 10 min, and concentrated. To the residue were added pyridine (10 mL) and acetic anhydride (10 mL), and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate/methanol, and the solution was subjected to silica gel column chromatography (NH, ethyl acetate). The solvent was evaporated, and the obtained solid was recrystallized (hexane/ethyl acetate) to give the title compound as white crystals (1.08 g).

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate)
  3. customto give a white solid
  4. stirringthe mixture was stirred at room temperature for 10 min
  5. concentrationconcentrated
  6. additionTo the residue were added pyridine (10 mL) and acetic anhydride (10 mL)
  7. stirringthe mixture was stirred at room temperature for 15 min
  8. concentrationThe reaction mixture was concentrated under reduced pressure
  9. dissolutionthe residue was dissolved in ethyl acetate/methanol
  10. customThe solvent was evaporated
  11. customthe obtained solid was recrystallized (hexane/ethyl acetate)

Sources & evidence

ORD record
ord-28e52c30a71b4780a0b231fad18a25a5
Source dataset
uspto-grants-2015_09
Patent number
US09133129B2

Reaction notes

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