Triethylamine → HCID 68940124, compound

HRID 1868975Notes

Reaction equation

HRID 1868975 reaction equation
[C:1]([O:4][C@@H:5]1[C@@H:10]([O:11][C:12](=[O:14])[CH3:13])[C@H:9]([O:15][C:16](=[O:18])[CH3:17])[C@@H:8]([CH2:19][O:20][C:21](=[O:23])[CH3:22])[O:7][C@H:6]1[O:24][C:25]1[C:29]([CH2:30][C:31]2[CH:36]=[CH:35][C:34]([O:37][CH2:38][CH2:39][CH2:40][NH2:41])=[CH:33][CH:32]=2)=[C:28]([CH:42]([CH3:44])[CH3:43])[NH:27][N:26]=1)(=[O:3])[CH3:2].C(N(CC)CC)C.Cl[C:53](OC1C=CC([N+]([O-])=O)=CC=1)=[O:54].[NH2:65][CH2:66][CH2:67][N:68]1[CH2:73][CH2:72][O:71][CH2:70][CH2:69]1>ClCCl.O>[C:1]([O:4][C@@H:5]1[C@@H:10]([O:11][C:12](=[O:14])[CH3:13])[C@H:9]([O:15][C:16](=[O:18])[CH3:17])[C@@H:8]([CH2:19][O:20][C:21](=[O:23])[CH3:22])[O:7][C@H:6]1[O:24][C:25]1[C:29]([CH2:30][C:31]2[CH:36]=[CH:35][C:34]([O:37][CH2:38][CH2:39][CH2:40][NH:41][C:53]([NH:65][CH2:66][CH2:67][N:68]3[CH2:73][CH2:72][O:71][CH2:70][CH2:69]3)=[O:54])=[CH:33][CH:32]=2)=[C:28]([CH:42]([CH3:44])[CH3:43])[NH:27][N:26]=1)(=[O:3])[CH3:2]

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 821294-Nitrophenyl chloroformateHCID 4082852-MorpholinoethylamineHCID 68937787HCID 68937787, compound

Product 1

HCID 68940124HCID 68940124, compoundYield 47.8%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of 3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-4-{[4-(3-aminopropoxy)phenyl]methyl}-5-isopropyl-1H-pyrazole (97 mg) in dichloromethane (3 mL) were added triethylamine (0.035 mL) and 4-nitrophenyl chloroformate (35 mg), and the mixture was stirred at room temperature for 1 hour. To the reaction mixture was added 4-(2-aminoethyl)morpholine (41 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, a saturated aqueous sodium hydrogen carbonate solution, water and brine successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate-dichloromethane/methanol=10/1-5/1) to give 3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-5-isopropyl-4-{[4-(3-{3-[2-(morpholin-4-yl)ethyl]ureido}propoxy)phenyl]-methyl}-1H-pyrazole (58 mg). This material was dissolved in methanol (3 mL). To the solution was added sodium methoxide (28% methanol solution, 0.03 mL), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue was purified by solid phase extraction on ODS (washing solvent: distilled water, eluent: methanol) to give the title compound (39 mg).

Workup

  1. stirringthe mixture was stirred at room temperature overnight
  2. extractionthe resulting mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materiala saturated aqueous sodium hydrogen carbonate solution, water and brine successively, dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel (eluent: ethyl acetate-dichloromethane/methanol=10/1-5/1)

Sources & evidence

ORD record
ord-e200d078e741443d8079d9d3a83f4585
Source dataset
uspto-grants-2009_12
Patent number
US07635684B2

Reaction notes

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