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Dimethylamine, hydrochloride → Dimethyl-(1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)-amine

HRID 269485
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HRID 269485 반응식
[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([CH:10]=O)[CH:9]=[C:4]2[CH:3]=[CH:2]1.Cl.[CH3:13][NH:14][CH3:15].[OH-].[Na+].C([BH3-])#N.[Na+]>CO.O>[CH3:13][N:14]([CH3:15])[CH2:10][C:8]1[CH:9]=[C:4]2[CH:3]=[CH:2][NH:1][C:5]2=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 10473Dimethylamine, hydrochlorideHCID 14798Sodium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 228320511H-Pyrrolo[2,3-b]pyridine-5-carbaldehyde

생성물 1

HCID 59832309Dimethyl-(1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)-amine수율 33%

시약·촉매·용매 2

HCID 887Methanol용매

실험 절차

To 1H-Pyrrolo[2,3-b]pyridine-5-carbaldehyde (114 mg, 0.78 mmol), in methanol (10 ml) was added dimethylamine hydrochloride (127 mg, 1.56 mmol, NaOH (31.2 mg, 0.78 mmol), sodium cyanoborohydride (49 mg, 0.78 mmol) and the solution was stirred under nitrogen for 12 hr. Poured into water (50 mL), extracted with ethyl acetate, dried (Na2SO4) to afforded Dimethyl-(1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)-amine (44 mg, 33% yield) used without purification. MS: m/e 176.1 (M+H).

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialdried (Na2SO4)

출처 및 근거

ORD 기록
ord-40b9bc0a873a44b18533dfd18f6659b6
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07446199B2

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