Water → HCID 70173263, compound

HRID 2304861Notes

Reaction equation

HRID 2304861 reaction equation
[C:1]([N:8]1[C:12]([C:13]([O:15]C)=[O:14])=[CH:11][O:10][CH:9]1[C@H:17]([NH2:26])[CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C(=O)([O-])[O-].[K+].[K+].O>CO.O>[C:1]([N:8]1[C:12]([C:13]([OH:15])=[O:14])=[CH:11][O:10][CH:9]1[C@H:17]([NH2:26])[CH2:18][CH2:19][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)([O:3][C:4]([CH3:6])([CH3:7])[CH3:5])=[O:2]

Participants

5

Procedure

A solution of methyl N-Boc-2-[(1R)-1-amino-3-phenylpropyl]-4-oxazolecarboxylate (388 mg) and potassium carbonate (1.5 g) in 90% methanol/water (10 mL) is brought to gentle reflux for 40 min. The reaction mixture is cooled, water is added and extracted thrice with ethyl acetate. The aqueous layer is acidified to pH 3 and extracted three times with ethyl acetate. The combined organic layer is washed twice with brine, dried (Na2SO4) and concentrated. The crude title product (372 mg) was >95% pure by NMR: 1H NMR (400 MHz, CDCl3) δ 1.41 (s, 9H), 2.18 (m, 1H), 2.22 (m, 1H), 2.69 (m, 2H), 5.01 (m, 1H), 5.88 (bs, 1H, NH), 7.16 (m, 3H), 7.23 (m, 2H), and 8.01 (s, 1H).

Workup

  1. temperatureto gentle reflux for 40 min
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted thrice with ethyl acetate
  4. extractionextracted three times with ethyl acetate
  5. washThe combined organic layer is washed twice with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-e9aaeeb65d5e497b829fee07084ebc5a
Source dataset
uspto-grants-2002_08
Patent number
US06436980B1

Reaction notes

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