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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aluminium lithium hydride → (1-Cyclopropyl-1H-indazol-5-yl) methanol

HRID 73107
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반응식

HRID 73107 반응식
[CH:1]1([N:4]2[C:12]3[C:7](=[CH:8][C:9]([C:13](OC)=[O:14])=[CH:10][CH:11]=3)[CH:6]=[N:5]2)[CH2:3][CH2:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH:1]1([N:4]2[C:12]3[C:7](=[CH:8][C:9]([CH2:13][OH:14])=[CH:10][CH:11]=3)[CH:6]=[N:5]2)[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 66837925Methyl 1-cyclopropyl-1H-indazole-5-carboxylate

생성물 1

HCID 66837867(1-Cyclopropyl-1H-indazol-5-yl) methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of methyl 1-cyclopropyl-1H-indazole-5-carboxylate (400 mg, 1.8 mmol, step-1 of Example 28) in THF (15 mL) was added LiAlH4 (70 mg, 1.8 mmol) at 0° C. The reaction mixture was stirred for 1 hr at room temperature, and quenched with saturated aqueous NH4Cl (20 mL). The mixture was diluted with DCM (80 mL), dried over Na2SO4, filtered through a pad of Celite (registered trademark) the filtrate was concentrated to give 386 mg (quant.) of the titled compound as pale yellow oil.

후처리

  1. customquenched with saturated aqueous NH4Cl (20 mL)
  2. additionThe mixture was diluted with DCM (80 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered through a pad of Celite (registered trademark) the filtrate
  5. concentrationwas concentrated

출처 및 근거

ORD 기록
ord-ffe41fb35518440f99abb7e853bdc907
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829026B2

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