Sodium Acetate → HCID 86654801, 화합물

HRID 521530노트

반응식

HRID 521530 반응식
[CH:1]([C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:6]([OH:8])=O)=[O:2].Cl.[CH3:15][O:16][C:17]([C:19]1([NH2:28])[CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH2:20]1)=[O:18].C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH3:15][O:16][C:17]([C:19]1([NH:28][C:6](=[O:8])[C:5]2[CH:9]=[CH:10][C:11]([O:12][CH3:13])=[C:3]([CH:1]=[O:2])[CH:4]=2)[CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH2:20]1)=[O:18]

참가 물질

5

반응물 3

HCID 517045Sodium AcetateHCID 190399693-Formyl-4-methoxybenzoic acidHCID 45074056methyl 2-amino-2,3-dihydro-1H-indene-2-carboxylate hydrochloride

생성물 1

HCID 86654801HCID 86654801, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

3-Formyl-4-methoxy-benzoic acid (F. D. Chattaway and F. Calvet, J. Chem. Soc. (1928), 2913-2918) (1.017 g, 5.65 mmol) was reacted with 2-amino-indane-2-carboxylic acid methyl ester hydrochloride in analogy to step 4 of example 3. The obtained product (1.895 g) was dissolved in acetic acid (20 ml), sodium acetate (0.57 g, 6.96 mmol) was added and the mixture was stirred under reflux for 24 h. The volatiles were evaporated in vacuo, the residue partitioned between a saturated sodium hydrogencarbonate solution and EA, and the aqueous phase extracted with EA. The combined organic phases were dried over sodium sulfate and evaporated to dryness to yield 1.52 g of the title compound.

후처리

  1. temperatureunder reflux for 24 h
  2. customThe volatiles were evaporated in vacuo
  3. customthe residue partitioned between a saturated sodium hydrogencarbonate solution and EA
  4. extractionthe aqueous phase extracted with EA
  5. dry with materialThe combined organic phases were dried over sodium sulfate
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-815455bc569a4d7ca80ecaaa5701bee1
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09328071B2

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