Sodium Hydroxide → HCID 59616761, compound

HRID 1470988Notes

Reaction equation

HRID 1470988 reaction equation
[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[C@@H:3]([C:8]([O:10]CC)=[O:9])[NH:2]2.[CH3:13][O:14][C:15]([NH:17][C@@H:18]([CH:22]([CH3:24])[CH3:23])[C:19](O)=[O:20])=[O:16].C(N(C(C)C)CC)(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[OH-].[Na+]>CN(C)C=O.O.C(O)C>[CH3:13][O:14][C:15]([NH:17][C@@H:18]([CH:22]([CH3:24])[CH3:23])[C:19]([N:2]1[C@H:3]([C:8]([OH:10])=[O:9])[CH:4]2[CH2:7][CH:1]1[CH2:6][CH2:5]2)=[O:20])=[O:16]

Participants

9

Procedure

(3S)-ethyl 2-azabicyclo[2.2.1]heptane-3-carboxylate (1.25 g, 7.39 mmol), (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (1.42 g, 8.13 mmol), diisopropylethylamine (6.45 mL, 36.9 mmol), and HATU (2.95 g, 7.76 mmol) were combined in dimethylformamide (40 mL) at ambient temperature and stirred for 2 hours. The solution was diluted with water and the product filtered and dried. The dried ester (1.0 g, 3.06 mmol) was taken up in water (15 mL) and ethanol (15 mL) and treated with sodium hydroxide (0.5 g, 12.5 mmol) at ambient temperature for 17 hours. The solution was washed with ether then the aqueous was neutralized with concentrated HCl to pH 7 and the product extracted into ethyl acetate, dried over sodium sulfate, and concentrated to give the title compound as a waxy solid.

Workup

  1. filtrationthe product filtered
  2. customdried
  3. washThe solution was washed with ether
  4. extractionthe product extracted into ethyl acetate
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-345ae96625fb489599ad76609fe5061f
Source dataset
uspto-grants-2015_04
Patent number
US09006387B2

Reaction notes

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