Triethylamine → 2-(Difluoromethyl)-5-[[(2-methyl-1-oxopropyl)amino]methyl]benzoic acid

HRID 241440노트

반응식

HRID 241440 반응식
[C:1](Cl)(=[O:5])[CH:2]([CH3:4])[CH3:3].Cl.[NH2:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([CH:20]([F:22])[F:21])=[C:14]([CH:19]=1)[C:15]([O:17]C)=[O:16].C(N(CC)CC)C.[OH-].[Na+]>C(Cl)Cl>[F:21][CH:20]([F:22])[C:13]1[CH:12]=[CH:11][C:10]([CH2:9][NH:8][C:1](=[O:5])[CH:2]([CH3:4])[CH3:3])=[CH:19][C:14]=1[C:15]([OH:17])=[O:16]

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 62325Isobutyryl chlorideHCID 67970562HCID 67970562, 화합물

생성물 1

HCID 679705062-(Difluoromethyl)-5-[[(2-methyl-1-oxopropyl)amino]methyl]benzoic acid수율 94.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Add isobutyryl chloride (0.571 mL, 5.42 mmol, 1.05 equiv) to a mixture of methyl 5-(aminomethyl)-2-(difluoromethyl)benzoate hydrochloride (1.30 g, 5.17 mmol, 1.0 equiv) and triethylamine (1.51 mL, 10.85 mmol, 2.1 equiv) in DCM (50 mL) at room temperature and stir the mixture for one hour. Dilute the mixture with DCM; wash with water; then with a saturated sodium chloride aqueous solution. Separate the organic layer; dry over sodium sulfate; filter; and concentrate the filtrate under reduced pressure. Dissolve the resulting crude material in 1,4-dioxane (10 mL), and add sodium hydroxide (5 N, 2 mL, 10 mmol, 1.93 equiv). Stir the resulting suspension at 40° C. overnight. Concentrate the mixture under reduced pressure, and treat the resulting residue with 1 N aqueous hydrochloric acid until the pH reaches 3. Extract the resulting suspension with EtOAc (2×30 mL). Wash the combined organic layers with a saturated sodium chloride aqueous solution (50 mL); dry over sodium sulfate; filter; and concentrate the filtrate under reduced pressure to give the title compound as a white solid (1.32 g, 94% yield). ES/MS (m/z) 272 (M+1).

후처리

  1. washwash with water
  2. customSeparate the organic layer
  3. dry with materialdry over sodium sulfate
  4. filtrationfilter
  5. concentrationand concentrate the filtrate under reduced pressure
  6. dissolutionDissolve the resulting crude material in 1,4-dioxane (10 mL)
  7. stirringStir the resulting suspension at 40° C. overnight
  8. concentrationConcentrate the mixture under reduced pressure
  9. additiontreat the resulting residue with 1 N aqueous hydrochloric acid until the pH
  10. extractionExtract the resulting suspension with EtOAc (2×30 mL)
  11. washWash the combined organic layers with a saturated sodium chloride aqueous solution (50 mL)
  12. dry with materialdry over sodium sulfate
  13. filtrationfilter
  14. concentrationand concentrate the filtrate under reduced pressure

출처 및 근거

ORD 기록
ord-26031bc8ecd74956892ec2428c3abe04
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08648200B2

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