Water → HCID 53893975, compound

HRID 1839468Notes

Reaction equation

HRID 1839468 reaction equation
[NH:1]1[CH2:9][CH2:8][CH2:7][CH:3]([C:4]([OH:6])=[O:5])[CH2:2]1.[OH-].[Na+].[CH2:12]([O:19][C:20]([NH:22][C:23](=[N:26][C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:28])SC)=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.O>O1CCOCC1.CCOCC>[CH2:30]([O:29][C:27]([NH:26][C:23](=[N:22][C:20]([O:19][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:21])[N:1]1[CH2:9][CH2:8][CH2:7][CH:3]([C:4]([OH:6])=[O:5])[CH2:2]1)=[O:28])[C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1

Participants

7

Procedure

To a solution of nipecotic acid (1.66 g, 12.8 mmol) in 2 N NaOH (12.8 mL, 25.6 mmol) and dioxane (30 mL) was added 1,3-bis(benzyloxycarbonyl)-2-methyl-2-thiopseudourea (4.6 g, 12.8 mmol). After 48 h, the reaction mixture was added to H2O (200 mL) and Et2O (200 mL). The aqueous layer was separated and extracted with Et2O (2×200 mL). The aqueous layer was acidified to pH, 2.0 with 3 N HCl and extracted with EtOAc (500 mL). The organic layer was MgSO4 dried and concentrated to give the title compound (4.0 g, 71%): TLC Rf=0.65 (1:15:135 Acetic Acid:Methanol:Chloroform); NMR (CDCl3) δ1.55-1.92 (m, 6H), 2.00-2.15 (m, 1H), 2.70-2.80 (m, 1H), 3.20-3.35 (q, 1H), 3.38-3.45 (m, 1H), 3.75-4.10 (m, 1H), 5.10 (s, 2H), 5.22 (s, 2H), 7.30-7.40 (m, 10H); FD-MS 440 (NH+).

Workup

  1. customThe aqueous layer was separated
  2. extractionextracted with Et2O (2×200 mL)
  3. extraction2.0 with 3 N HCl and extracted with EtOAc (500 mL)
  4. customdried
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-c6c3c561e0c94d6bb4154ab9d8ef52df
Source dataset
uspto-grants-2004_01
Patent number
US06677369B2

Reaction notes

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