HCID 66672612, compound → HCID 66673122, compound

HRID 1269397Notes

Reaction equation

HRID 1269397 reaction equation
[C:1]([O:4][CH2:5][C@@:6]([NH:27][C:28](=[O:30])[CH3:29])([CH3:26])[CH2:7][CH2:8][C:9]1[N:10]([CH3:25])[C:11]([C:14]#[C:15][CH2:16][CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:12][CH:13]=1)(=[O:3])[CH3:2]>CO.[Pd]>[C:1]([O:4][CH2:5][C@@:6]([NH:27][C:28](=[O:30])[CH3:29])([CH3:26])[CH2:7][CH2:8][C:9]1[N:10]([CH3:25])[C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[CH:12][CH:13]=1)(=[O:3])[CH3:2]

Participants

4

Reactant 1

HCID 66672612HCID 66672612, compound

Product 1

HCID 66673122HCID 66673122, compoundYield 97%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

To a solution of (2R)-1-acetoxy-2-acetylamino-2-methyl-4-[1-methyl-5-(5-phenylpent-1-ynyl)pyrrol-2-yl]butane (77 mg, 0.19 mmol) obtained in Example (31a) in methanol (2 ml) was added 10% palladium-charcoal (50% wet with water) (4.3 mg), and the resulting mixture was stirred at room temperature under a hydrogen atmosphere for 1 hour. After stirring, the internal atmosphere was replaced with nitrogen, and the palladium-charcoal in the reaction mixture was filtered off using celite, which was washed with ethyl acetate. The filtrate and the washings were combined and evaporated to dryness in vacuo to afford the title compound (75.5 mg, yield: 97%).

Workup

  1. stirringAfter stirring
  2. filtrationthe palladium-charcoal in the reaction mixture was filtered off
  3. washwas washed with ethyl acetate
  4. customevaporated to dryness in vacuo

Sources & evidence

ORD record
ord-fef4f1541b604a6eabf58b2d5b7898d0
Source dataset
uspto-grants-2007_04
Patent number
US07199150B2

Reaction notes

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