1-Aminocyclohexanecarboxylic acid → HCID 24740121, 화합물

HRID 73840

반응식

HRID 73840 반응식
[CH3:1][C:2]1[O:6][N:5]=[CH:4][C:3]=1[C:7]([OH:9])=O.S(Cl)(Cl)=O.[NH2:14][C:15]1([C:21](O)=[O:22])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1.C(=O)([O-])O.[Na+].Cl.C(N=C=NCCCN(C)C)C>C1(C)C=CC=CC=1.O>[CH3:1][C:2]1[O:6][N:5]=[CH:4][C:3]=1[C:7]1[O:9][C:21](=[O:22])[C:15]2([CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[N:14]=1

참가 물질

8

실험 절차

1 g (7.87 mmol) of 5-methylisoxazole-4-carboxylic acid was added to 3 ml of thionyl chloride, and the mixture was stirred overnight. Under reduced pressure, the reaction solution was concentrated, and the obtained residue was added to a solution of 1.13 g (7.87 mmol) of 1-aminocyclohexanecarboxylic acid and 6.6 g (79 mmol) of sodium hydrogencarbonate in 30 ml of toluene-30 ml of water. After the mixture was stirred at room temperature overnight, the toluene layer was separated. The aqueous layer was neutralized by potassium hydrogensulfate, and it was extracted with ethyl acetate. After the obtained organic layer was washed with saturated brine, it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, methylene chloride was added thereto, and under ice-cooling, 332 mg (1.73 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added. After the mixture was stirred at room temperature overnight, under reduced pressure, the reaction solution was concentrated, ethyl acetate was added thereto, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 295 mg (16%) of the title compound.

후처리

  1. concentrationUnder reduced pressure, the reaction solution was concentrated
  2. stirringAfter the mixture was stirred at room temperature overnight
  3. customthe toluene layer was separated
  4. extractionwas extracted with ethyl acetate
  5. washAfter the obtained organic layer was washed with saturated brine, it
  6. dry with materialwas dried with anhydrous sodium sulfate
  7. distillationThe solvent was distilled off under reduced pressure, methylene chloride
  8. additionwas added
  9. temperatureunder ice-cooling
  10. stirringAfter the mixture was stirred at room temperature overnight, under reduced pressure
  11. concentrationthe reaction solution was concentrated
  12. additionethyl acetate was added
  13. washthe mixture was successively washed with water
  14. dry with materialby drying with anhydrous sodium sulfate
  15. distillationThe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-2a330b4be3674c6681db8055d377aa19
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08829209B2

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