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N-Methyl dicyclohexylamine → 5-bromo-7-methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole

HRID 469305
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반응식

HRID 469305 반응식
Cl[CH2:2][O:3][CH2:4][CH2:5][Si:6]([CH3:9])([CH3:8])[CH3:7].[Br:10][C:11]1[CH:12]=[C:13]2[C:17](=[C:18]([CH3:20])[CH:19]=1)[NH:16][N:15]=[CH:14]2.CN(C1CCCCC1)C1CCCCC1>C1COCC1>[Br:10][C:11]1[CH:12]=[C:13]2[C:17](=[C:18]([CH3:20])[CH:19]=1)[N:16]([CH2:2][O:3][CH2:4][CH2:5][Si:6]([CH3:9])([CH3:8])[CH3:7])[N:15]=[CH:14]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24210N-Methyl dicyclohexylamineHCID 13820335-Bromo-7-methyl-1H-indazoleHCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl ether

생성물 1

HCID 581812085-bromo-7-methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

1.95 mL (11.0 mmol) (2-chloromethoxy-ethyl)-trimethyl-silane were added to 2.11 g (10.0 mmol) 5-bromo-7-methyl-1H-indazole and 1.80 mL (12.3 mmol) N-methyldicyclohexylamine in 50 mL THF and stirred overnight at RT. The precipitate formed was filtered off and the filtrate was evaporated down. The residue was purified by flash chromatography.

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후처리

  1. customThe precipitate formed
  2. filtrationwas filtered off
  3. customthe filtrate was evaporated down
  4. customThe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-bb0ef38bd3d1402b842c1a6df6a14b57
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629137B2

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