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Potassium Hydroxide → HCID 16100379, 화합물

HRID 1361427
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HRID 1361427 반응식
C[O:2][C:3](=[O:23])[C:4]([CH3:22])([N:6]1[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][N:13]=2)[CH2:8][CH2:7]1)[CH3:5].[OH-].[K+]>O1CCOCC1>[CH3:22][C:4]([N:6]1[CH2:7][CH2:8][N:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:20])([F:21])[F:19])=[CH:14][N:13]=2)[CH2:10][CH2:11]1)([CH3:5])[C:3]([OH:23])=[O:2]
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 16100378HCID 16100378, 화합물

생성물 1

HCID 16100379HCID 16100379, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
60 °C

실험 절차

A solution of 2-methyl-2-[4-(5-trifluoromethyl-pyridin-2-yl)-piperazin-1-yl]-propionic acid methyl ester (1.05 g, 3.17 mmoles) from Example 14B in dioxane (10 mL) was treated with 5N potassium hydroxide (10 mL) and stirred for 4 hours at 60° C. The dioxane was removed under reduced pressure, the residue was neutralized with 1N HCl to pH=7 and extracted three times with 4:1 THF:DCM. The combined organic extracts were dried (MgSO4), filtered and the filtrate concentrated under reduced pressure to provide the title compound as a white solid.

후처리

  1. customThe dioxane was removed under reduced pressure
  2. extractionextracted three times with 4:1 THF
  3. dry with materialThe combined organic extracts were dried (MgSO4)
  4. filtrationfiltered
  5. concentrationthe filtrate concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-381bb90ab8b743d3ba62fed011871182
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07880001B2

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