Hydrochloric Acid → 2-[3-(2-m-Tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

HRID 1810882노트

반응식

HRID 1810882 반응식
[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]

참가 물질

8

반응물 6

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

생성물 1

HCID 670766442-[3-(2-m-Tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester수율 43.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-07bc851968b445d5a46c3fb3cbda1dfb
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362073B2

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