Triethylamine → HCID 18414408, compound

HRID 991944Notes

Reaction equation

HRID 991944 reaction equation
CC1[N:3]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]3[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH2:22])=[CH:16][CH:15]=3)[N:9]=2)C(C)=CC=1.[C:23]1([CH:29](C)[CH2:30][C:31](O)=O)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[CH3:35]CN=C=NCCCN(C)C.C(N(CC)CC)C.C([O-])(=O)CC(CC([O-])=O)(C([O-])=O)O>C(#N)C>[C:23]1([CH2:29][CH2:30][CH2:31][CH2:35][NH:22][CH2:21][CH2:20][C:17]2[CH:16]=[CH:15][C:14]([C:10]3[N:9]=[C:8]([NH2:3])[CH:13]=[CH:12][CH:11]=3)=[CH:19][CH:18]=2)[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

Participants

7

Procedure

N-(2-(2, 5-Dimethylpyrrol-1-yl)-6-ethyl]-phenyl}-pyridyl)-(3-phenylbutyramide): To a 100 mL round-bottomed flask equipped with N2 inlet were added 200 mg (0.687 mmol) 2-(2, 5-dimethylpyrrol-1-yl)-6-(4-(2-aminoethyl)phenyl)-pyridine (Example 100D), 113 mg (0.687 mmol) 3-phenylbutyric acid, 132 mg (0.687 mmol) EDAC, 10 mg N-hydroxybenzot-iazole, 5 mL dry acetonitrile, and 211 uL (1.51 mmol) triethylamine. The reaction was stirred at room temperature for 12 h, poured into dilute aqueous citrate solution, and extracted into ethyl acetate. The organic layer was washed with water, aqueous sodium bicarbonate solution, and brine, dried over sodium sulfate, and evaporated. The resulting yellow oil, 300 mg (100%) was used directly.

Workup

  1. customTo a 100 mL round-bottomed flask equipped with N2 inlet
  2. extractionextracted into ethyl acetate
  3. washThe organic layer was washed with water, aqueous sodium bicarbonate solution, and brine
  4. dry with materialdried over sodium sulfate
  5. customevaporated

Sources & evidence

ORD record
ord-0503f6545e9d4dd89470feeca8aa5a99
Source dataset
uspto-grants-2002_10
Patent number
US06465491B2

Reaction notes

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