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Fumaric Acid → Votracon

HRID 1658381
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HRID 1658381 반응식
[C:1]([OH:9])(=[O:8])[CH:2]([CH2:4][C:5]([OH:7])=[O:6])O.[NH2:10][C:11]1[CH:31]=[CH:30][C:14]([C:15]([N:17]([CH:19]2[CH2:23][CH2:22][N:21]([CH:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)[CH2:20]2)[CH3:18])=[O:16])=[CH:13][CH:12]=1.C(O)(=O)/C=C/C(O)=O>C(Cl)(Cl)Cl>[C:1]([OH:9])(=[O:8])/[CH:2]=[CH:4]/[C:5]([OH:7])=[O:6].[NH2:10][C:11]1[CH:12]=[CH:13][C:14]([C:15]([N:17]([CH:19]2[CH2:23][CH2:22][N:21]([CH:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)[CH2:20]2)[CH3:18])=[O:16])=[CH:30][CH:31]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 444972Fumaric AcidHCID 12895722HCID 12895722, 화합물

생성물 1

HCID 5384146Votracon

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

An aqueous solution containing 3.9 g. (0.0094 mole) of (-) 4-amino-N-(1-cyclohexyl-3-pyrrolidinyl)-N-methylbenzamide malate (Example 68) was extracted with chloroform, the chloroform solution was dried over sodium sulfate and concentrated. The residue was dissolved in ethanol, 1.2 g. (0.01 mole) of fumaric acid added and the solution refrigerated. The fumarate salt which separated weighed 3.3 g. and melted at 205°-207°C. [α]D30 = - 13.89.

후처리

addition
An aqueous solution containing 3.9 g
  • dry with materialthe chloroform solution was dried over sodium sulfate
  • concentrationconcentrated
  • dissolutionThe residue was dissolved in ethanol
  • customThe fumarate salt which separated
  • 출처 및 근거

    ORD 기록
    ord-c04d89058e2c476193f4eb596c14bcac
    출처 데이터셋
    uspto-grants-1976_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03963745

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