Acetic Anhydride → HCID 59909957, compound

HRID 2117007Notes

Reaction equation

HRID 2117007 reaction equation
[C:1]([NH:8][C@H:9]([C:18]([NH2:20])=[O:19])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:21](OC(=O)C)(=[O:23])[CH3:22]>N1C=CC=CC=1>[C:4]([O:3][C:1]([NH:8][C@H:9]([C:18](=[O:19])[NH2:20])[CH2:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][C:21](=[O:23])[CH3:22])=[CH:15][CH:16]=1)=[O:2])([CH3:5])([CH3:7])[CH3:6]

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 11022297HCID 11022297, compound

Product 1

HCID 59909957HCID 59909957, compoundYield 86.6%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

To a solution of Boc-tyrosine amide (0.960 g, 3.4 mmol) in pyridine (10 mL) stirred under argon was added acetic anhydride (808 μL, 8.56 mmol). After 18 hrs of stirring the solvent was evaporated, the residue taken in EtOAc (30 mL) washed with 5% aqueous citric acid (3×20 mL) and brine. The solution was dried (MgSO4) and the solvent evaporated to yield 949 mg (86%) of the title compound.

Workup

  1. customwas evaporated
  2. washwashed with 5% aqueous citric acid (3×20 mL) and brine
  3. dry with materialThe solution was dried (MgSO4)
  4. customthe solvent evaporated

Sources & evidence

ORD record
ord-fabc4c8f5d904275aaef235a1aca7e12
Source dataset
uspto-grants-2008_10
Patent number
US07439258B2

Reaction notes

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