Water → HCID 57263458, compound

HRID 1737020Notes

Reaction equation

HRID 1737020 reaction equation
C(N(CC)CC)C.[C:8](Cl)(=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:17]([C@@H:24]1[CH2:29][C@@H:28]([N:30]([CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[N:41]=[CH:40][CH:39]=2)[C:31](=[O:36])[C:32]([F:35])([F:34])[F:33])[CH2:27][CH2:26][NH:25]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.O>C(Cl)Cl>[CH2:17]([C@@H:24]1[CH2:29][C@@H:28]([N:30]([CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[N:41]=[CH:40][CH:39]=2)[C:31](=[O:36])[C:32]([F:34])([F:35])[F:33])[CH2:27][CH2:26][N:25]1[C:8](=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

6

Procedure

72 μl (0.515 mmol) of triethylamine and 54 μl (0.468 mmol) of benzoyl chloride are added to a solution of 200 mg (0.468 mmol) of (2R*,4S*)-2-benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine in 4 ml of methylene chloride. The reaction mixture is stirred at 0° for 3 hours, water is added, extraction with methylene chloride is carried out. The organic phases are dried over magnesium sulfate and evaporated to dryness. The yellow oil is chromatographed on silica gel with methylene chloride/methanol/conc. ammonia (1000:50:1). The title compound is obtained as white foam. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.72, FD-MS: M+ =531.

Workup

  1. extractionextraction with methylene chloride
  2. dry with materialThe organic phases are dried over magnesium sulfate
  3. customevaporated to dryness
  4. customThe yellow oil is chromatographed on silica gel with methylene chloride/methanol/conc

Sources & evidence

ORD record
ord-761526f02b0d4938a310ace2e066f835
Source dataset
uspto-grants-1996_07
Patent number
US05541195

Reaction notes

Loading…