Water → HCID 69018038, compound

HRID 133828Notes

Reaction equation

HRID 133828 reaction equation
[C:1]([O:5][C:6]([N:8]([CH3:42])[C@@H:9]([C:33]([CH3:41])([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)[CH3:34])[CH2:10][NH:11][C@H:12]([C:17]([N:19]([CH3:32])[C@@H:20]([CH:29]([CH3:31])[CH3:30])/[CH:21]=[C:22](\[CH3:28])/[C:23]([O:25]CC)=[O:24])=[O:18])[C:13]([CH3:16])([CH3:15])[CH3:14])=[O:7])([CH3:4])([CH3:3])[CH3:2].O1CCCC1.O.[OH-].[Li+]>CO>[C:1]([O:5][C:6]([N:8]([CH3:42])[C@@H:9]([C:33]([CH3:41])([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)[CH3:34])[CH2:10][NH:11][C@H:12]([C:17]([N:19]([CH3:32])[C@@H:20]([CH:29]([CH3:31])[CH3:30])/[CH:21]=[C:22](\[CH3:28])/[C:23]([OH:25])=[O:24])=[O:18])[C:13]([CH3:16])([CH3:15])[CH3:14])=[O:7])([CH3:2])([CH3:3])[CH3:4]

Participants

6

Procedure

Ethyl (2E,4S)-4-[(N-{(2S)-2-[(tert-butoxycarbonyl)(methyl)amino]-3-methyl-3-phenyl butyl}-3-methyl-L-valyl)(methyl)amino]-2,5-dimethyl-2-hexenoate (50 mg, 0.085 mmol, Reference Example 20) is dissolved in methanol (1 ml), tetrahydrofuran (1 ml). To this solution is added water (0.5 ml) and solid lithium hydroxide (4.1 mg). The resulting mixture is stirred at room temperature for 15 hours. The organic solvents are removed in vacuo, and the residual aqueous mixture is cooled with an ice water bath, and acidified to pH 5.5-6.0 with aqueous 1 N aqueous citric acid solution. The precipitate is collect by filtration, and the solid is washed with a cold water, and dried over high vacuum. Alternatively, the product can be purified by using preparative HPLC. (40 mg, 80%) MS [M+H] 588.2

Workup

  1. customThe organic solvents are removed in vacuo
  2. temperaturethe residual aqueous mixture is cooled with an ice water bath
  3. filtrationThe precipitate is collect by filtration
  4. washthe solid is washed with a cold water
  5. customdried over high vacuum
  6. customAlternatively, the product can be purified

Sources & evidence

ORD record
ord-f594f92cf5e0451ca7682c624c2f26ce
Source dataset
uspto-grants-2008_06
Patent number
US07390910B2

Reaction notes

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