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HCID 70045178, 화합물 → Ranolazine

HRID 1285543
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HRID 1285543 반응식
C(O)(=O)C.[CH3:5][O:6][C:7]1[CH:35]=[CH:34][CH:33]=[CH:32][C:8]=1[O:9][CH2:10][CH:11]([OH:31])[CH2:12][N:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]([NH:22][C:23]2[C:28]([CH3:29])=[CH:27][CH:26]=[CH:25][C:24]=2[CH3:30])=[O:21])[CH2:15][CH2:14]1>S(=O)(=O)(O)O>[CH3:5][O:6][C:7]1[CH:35]=[CH:34][CH:33]=[CH:32][C:8]=1[O:9][CH2:10][CH:11]([OH:31])[CH2:12][N:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]([NH:22][C:23]2[C:24]([CH3:30])=[CH:25][CH:26]=[CH:27][C:28]=2[CH3:29])=[O:21])[CH2:15][CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 70045178HCID 70045178, 화합물

생성물 1

HCID 56959Ranolazine

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

1-[3-(2-methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine acetate (1.0 g) is dissolved in 50 ml 50% aqueous sulfuric acid, and the solution evaporated to dryness. The product is suspended in ethanol and filtered, air dried and recrystallized from methanol/acetone to yield 1-[3-(2-methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine.2HSO4.

후처리

  1. customthe solution evaporated to dryness
  2. filtrationfiltered
  3. customair dried
  4. customrecrystallized from methanol/acetone

출처 및 근거

ORD 기록
ord-ce7bed6fb8e44959a6805bcaab383297
출처 데이터셋
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04567264

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