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Sodium Hydroxide → 3-[2-(1-Isopropylcarbamoyl-piperidin-4-yl)ethoxy]-benzoic acid

HRID 2194636
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HRID 2194636 반응식
[CH:1]([NH:4][C:5]([N:7]1[CH2:12][CH2:11][CH:10]([CH2:13][CH2:14][O:15][C:16]2[CH:17]=[C:18]([CH:24]=[CH:25][CH:26]=2)[C:19]([O:21]CC)=[O:20])[CH2:9][CH2:8]1)=[O:6])([CH3:3])[CH3:2].[OH-].[Na+]>C(O)C>[CH:1]([NH:4][C:5]([N:7]1[CH2:12][CH2:11][CH:10]([CH2:13][CH2:14][O:15][C:16]2[CH:17]=[C:18]([CH:24]=[CH:25][CH:26]=2)[C:19]([OH:21])=[O:20])[CH2:9][CH2:8]1)=[O:6])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 66929612Ethyl 3-[2-(1-isopropylcarbamoyl-piperidin-4-yl)-ethoxy]-benzoate

생성물 1

HCID 669297103-[2-(1-Isopropylcarbamoyl-piperidin-4-yl)ethoxy]-benzoic acid

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
20 °C

실험 절차

Ethyl 3-[2-(1-isopropylcarbamoyl-piperidin-4-yl)-ethoxy]-benzoate (0.67 g, 1.8 mmol) was dissolved in ethanol (25 ml), wereupon NaOH (1 N, 10 ml) was added, and the solution was stirred overnight at 20° C. The reaction mixture was concentrated in vacuo, dissolved in HCl (1 N, 25 ml) and the resulting solution was extracted with EtOAc (3×25 ml). The combined organic extracts were dried (MgSO4) and evaporated to give 0.62 of the title compound. LC-MS (m/z): 336 (M+2).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutiondissolved in HCl (1 N, 25 ml)
  3. extractionthe resulting solution was extracted with EtOAc (3×25 ml)
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. customevaporated

출처 및 근거

ORD 기록
ord-965c7145378e491a8586033266e96262
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08334305B2

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