Hydrochloric Acid → HCID 67076644, compound

HRID 1810882Notes

Reaction equation

HRID 1810882 reaction equation
[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:30])[C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[C:18]([O:26][C:27](=O)[CH3:28])[CH:17]=2)[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[O:4].C(=O)([O-])[O-].[K+].[K+].Cl.[CH3:38][C:39]1[CH:40]=[C:41](CCO)[CH:42]=[CH:43][CH:44]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C>CO>[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:30])[C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:23])([F:25])[F:24])=[C:18]([O:26][CH2:27][CH2:28][C:43]3[CH:44]=[C:39]([CH3:38])[CH:40]=[CH:41][CH:42]=3)[CH:17]=2)[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[O:4]

Participants

8

Reactant 6

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 11776TriphenylphosphineHCID 746483-MethylbenzeneethanolHCID 5363146Diisopropyl azodicarboxylateHCID 670766942-(3-Acetoxy-4-trifluoromethyl-benzoylamino)-indane-2-carboxylic acid methyl ester

Product 1

HCID 67076644HCID 67076644, compoundYield 43.6%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

200 mg (0.48 mmol) of the compound of step 2 were dissolved in 5 ml of methanol, 13.1 mg (0.1 mmol) of potassium carbonate were added and the mixture was stirred for 30 min. The mixture was acidified with 1 N hydrochloric acid and extracted three times with 20 ml portions of EA. The combined organic phases were dried and evaporated. The residue was dissolved in 5 ml of THF, 96.9 mg (0.71 mmol) of 2-(3-methylphenyl)-ethanol and 186.7 mg (0.71 mmol) of triphenylphosphine were added, the mixture was cooled in an ice bath, and 191.9 mg (0.95 mmol) of DIAD were added. After stirring overnight, the mixture was evaporated to dryness and the residue was purified by preparative RP HPLC (water/ACN gradient). 104 mg of the title compound were obtained.

Workup

  1. extractionextracted three times with 20 ml portions of EA
  2. customThe combined organic phases were dried
  3. customevaporated
  4. dissolutionThe residue was dissolved in 5 ml of THF
  5. temperaturethe mixture was cooled in an ice bath
  6. stirringAfter stirring overnight
  7. customthe mixture was evaporated to dryness
  8. customthe residue was purified by preparative RP HPLC (water/ACN gradient)

Sources & evidence

ORD record
ord-07bc851968b445d5a46c3fb3cbda1dfb
Source dataset
uspto-grants-2013_01
Patent number
US08362073B2

Reaction notes

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