HCID 58022609, compound → HCID 58022560, compound

HRID 2389303Notes

Reaction equation

HRID 2389303 reaction equation
[CH2:1]([C@@:4]([NH:31][C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])([CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([S:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=2)=[CH:15][C:14]=1[Cl:30])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:2]=[CH2:3]>C(OCC)(=O)C.[Pd]>[C:35]([O:34][C:32]([NH:31][C@:4]([CH2:1][CH2:2][CH3:3])([CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([S:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:27])[F:28])[CH:21]=2)=[CH:15][C:14]=1[Cl:30])[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:33])([CH3:38])([CH3:36])[CH3:37]

Participants

4

Procedure

To a solution of the compound of Example 13 (400 mg) in ethyl acetate (20 mL) was added palladium, on activated carbon/ethylene diamine complex (100 mg), and the resultant solution was stirred at room temperature for 24 hours under hydrogen atmosphere. The reaction solution was filtered through Celite, and the solvent was evaporated. The resultant residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to obtain the target product (293 mg) as a colorless oil.

Workup

  1. filtrationThe reaction solution was filtered through Celite
  2. customthe solvent was evaporated
  3. customThe resultant residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1)

Sources & evidence

ORD record
ord-ca9bcf63f05e49d4a815fdd376fe17b2
Source dataset
uspto-grants-2012_09
Patent number
US08273748B2

Reaction notes

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