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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Potassium Carbonate → 3,4,5-Trimethylpyridin-2-amine

HRID 1910358
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HRID 1910358 반응식
[NH2:1][C:2]1[C:7]([CH3:8])=[C:6]([CH3:9])[C:5](Br)=[CH:4][N:3]=1.[CH3:11]B1OB(C)OB(C)O1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[NH2:1][C:2]1[C:7]([CH3:8])=[C:6]([CH3:9])[C:5]([CH3:11])=[CH:4][N:3]=1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 574072TrimethylboroxineHCID 70103075-Bromo-3,4-dimethylpyridin-2-amine

생성물 1

HCID 576746683,4,5-Trimethylpyridin-2-amine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
115 °C

실험 절차

23.0 g (0.11 mol) of 2-amino-5-bromo-3,4-dimethylpyridine was mixed with 14.1 g (0.11 mol) of trimethylboroxin (TMB), 12.9 g (0.011 mol) of Pd(Ph3)4, 46.0 g (0.33 mol) of K2CO3 and 220 mL of DMF. The reaction mixture was heated under nitrogen at 115° C. for 18 hours. The reaction mixture was purified by silica gel column. The desired product was confirmed by MS.

후처리

  1. customThe reaction mixture was purified by silica gel column

출처 및 근거

ORD 기록
ord-3f3edfe8ed484aabadaf12a1ead799a3
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08603645B2

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