Sodium Bicarbonate → HCID 68485154, compound

HRID 2170250Notes

Reaction equation

HRID 2170250 reaction equation
Cl.C(S[C:7]1[CH:8]=[C:9]([CH:13]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[CH2:14][NH:15][CH2:16][C:17]([N:19]([CH3:21])[CH3:20])=[O:18])[CH:10]=[CH:11][CH:12]=1)CCC.Cl.[CH2:30](SC1C=C(CCNCC(N(C)C)=O)C=CC=1)[CH2:31][CH2:32][CH3:33].O[O:51][S:52]([O-:54])=O.[K+].C([O-])(O)=O.[Na+]>C(#N)C.O>[CH2:30]([S:52]([C:7]1[CH:8]=[C:9]([CH:13]([C:22]([O:24][C:25]([CH3:27])([CH3:26])[CH3:28])=[O:23])[CH2:14][NH:15][CH2:16][C:17]([N:19]([CH3:20])[CH3:21])=[O:18])[CH:10]=[CH:11][CH:12]=1)(=[O:54])=[O:51])[CH2:31][CH2:32][CH3:33]

Participants

7

Procedure

To a solution of 2-[2-(3-butylthiophenyl)-(tert-butoxycarbonyl)ethylamino]-N,N-dimethylacetamide hydrochloride (0.25 g, 0.62 mmol; prepared from the compound of Step 2 of Example 7, by reaction with boc2O according to the procedure described in the first part of Step 1 of Example 1) in acetonitrile (20 ml)/water (10 ml), a mixture of oxone (0.92 g, 1.5 mmol) and NaHCO3 (0.2 g, 2.3 mmol) was added portionwise over 5 minutes. The mixture was stirred at room temperature for 2 h. The mixture was partitioned between water and CH2Cl2, the organic was washed with water and brine, dried over Na2SO4 and the solvent was evaporated under reduced pressure. The crude was purified by flash chromatography (petroleum ether:AcOEt 3:7) to give pure title compound as a colourless oil (0.20 g, 75% yield).

Workup

  1. additionwas added portionwise over 5 minutes
  2. customThe mixture was partitioned between water and CH2Cl2
  3. washthe organic was washed with water and brine
  4. dry with materialdried over Na2SO4
  5. customthe solvent was evaporated under reduced pressure
  6. customThe crude was purified by flash chromatography (petroleum ether:AcOEt 3:7)

Sources & evidence

ORD record
ord-1df40c8bc01947eb8c07c0de8c6d5644
Source dataset
uspto-grants-2015_06
Patent number
US09051240B2

Reaction notes

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