Hydrochloric Acid → HCID 11712533, compound

HRID 901788Notes

Reaction equation

HRID 901788 reaction equation
C([O:8][C@@H:9]1[C@@H:47]([O:48]CC2C=CC=CC=2)[C@H:46]([O:56][C@@H:57]2[O:86][C@H:85]([CH2:87][O:88][CH3:89])[C@@H:76]([O:77]CC3C=CC=CC=3)[C@H:67]([O:68]CC3C=CC=CC=3)[C@H:58]2[O:59]CC2C=CC=CC=2)[C@@H:45]([CH2:90][O:91]CC2C=CC=CC=2)[O:44][C@@H:10]1[O:11][C@H:12]1[C@H:16]([O:17]CC2C=CC=CC=2)[CH2:15][N:14](C(OCC2C=CC=CC=2)=O)[C@@H:13]1[CH2:35][O:36]CC1C=CC=CC=1)C1C=CC=CC=1.Cl>CO.[OH-].[Pd+2].[OH-].[C]>[CH3:89][O:88][CH2:87][C@H:85]1[O:86][C@@H:57]([O:56][C@@H:46]2[C@@H:45]([CH2:90][OH:91])[O:44][C@H:10]([O:11][C@H:12]3[C@H:16]([OH:17])[CH2:15][NH:14][C@@H:13]3[CH2:35][OH:36])[C@H:9]([OH:8])[C@H:47]2[OH:48])[C@H:58]([OH:59])[C@@H:67]([OH:68])[C@@H:76]1[OH:77]

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 86602934HCID 86602934, compound

Product 1

HCID 11712533HCID 11712533, compoundYield 95%

Reagents, catalysts & solvents 2

HCID 178502593HCID 178502593, compoundCatalystHCID 887MethanolSolvent

Procedure

The compound (150.1 mg, 0.11 mmol) synthesized in Example 8 (8c) was dissolved in methanol (10 mL) containing 1% aqueous hydrochloric acid solution and 20% palladium hydroxide-carbon (100 mg) was added thereto, followed by stirring of the mixture under a hydrogen atmosphere for 2 hours. After the catalyst was removed by celite filtration, 28% ammonia water (0.5 mL) was added thereto and the mixture was stirred for 10 minutes. After the solvent was distilled off under reduced pressure and the aqueous solution (100 mL) was subjected to ion exchange resin (Dowex 50w×8) column, it was eluted with 1% ammonia water (100 mL). The ammonia water containing the desired compound was concentrated under reduced pressure and the residue was purified using silica gel flash column chromatography (ethyl acetate:methanol:water, 5:2:1-1:1:1, V/V) to obtain the desired title compound (49.1 mg, 95%) as a colorless solid.

Workup

  1. additionwas added
  2. customAfter the catalyst was removed by celite filtration, 28% ammonia water (0.5 mL)
  3. additionwas added
  4. stirringthe mixture was stirred for 10 minutes
  5. distillationAfter the solvent was distilled off under reduced pressure
  6. washwas eluted with 1% ammonia water (100 mL)
  7. concentrationThe ammonia water containing the desired compound was concentrated under reduced pressure
  8. customthe residue was purified

Sources & evidence

ORD record
ord-ccf8f171585542fd86af5a1bff75edb8
Source dataset
uspto-grants-2008_04
Patent number
US07361744B2

Reaction notes

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