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Hydrochloric Acid → 1-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxylic acid

HRID 62443
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HRID 62443 반응식
[CH3:1][N:2]1[C:10]2[CH2:9][CH2:8][CH2:7][CH:6]([C:11]([O-:13])=[O:12])[C:5]=2[CH:4]=[N:3]1.[Li+].[OH-].Cl>CO.C1COCC1.O>[CH3:1][N:2]1[C:10]2[CH2:9][CH2:8][CH2:7][CH:6]([C:11]([OH:13])=[O:12])[C:5]=2[CH:4]=[N:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 1317371911-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxylate

생성물 1

HCID 772303371-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxylic acid수율 94%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a solution of 1-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxylate (7 g, 36 mmol) in methanol (100 mL), THF (50 mL) and H2O (50 mL) was added LiOH (2.5 g, 108 mmol). The resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was acidified with 1N HCl solution to pH=5-6, and extracted with EA three times. The combined organic layers were washed with brine, dried over Na2SO4. The solvent was concentrated to give 1-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxylic acid (6 g, 94%), which was used in the next step directly.

후처리

  1. extractionextracted with EA three times
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationThe solvent was concentrated

출처 및 근거

ORD 기록
ord-fd084183767c4a3fbb410b56931aa556
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09446130B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매