홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Thionyl Chloride → 5-Bromo-N-methylpyridine-2-carboxamide

HRID 2361646
노트
인쇄 미리보기

반응식

HRID 2361646 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([OH:10])=O)=[N:6][CH:7]=1.S(Cl)(Cl)=O.Cl.CN.C[CH2:19][N:20](C(C)C)C(C)C>C1(C)C=CC=CC=1.ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([NH:20][CH3:19])=[O:10])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 24386Thionyl ChlorideHCID 81531DiisopropylethylamineHCID 6085445-Bromopyridine-2-carboxylic acidHCID 6364545Methylamine hydrochloride

생성물 1

HCID 228316205-Bromo-N-methylpyridine-2-carboxamide수율 63.2%

시약·촉매·용매 2

HCID 1140Toluene
용매
HCID 6344Dichloromethane용매

실험 절차

5-Bromo-pyridine-2-carboxylic acid (2.59 g, 12.8 mmol) and thionylchloride (2.79 ml) were heated at reflux in toluene (25 ml) for 16 hours. Excess reagents were removed in vacuo and the residue was diluted in dichloromethane (50 ml). A mixture of methyl amine hydrochloride (2.60 g, 38.5 mmol) and DIPEA (6.7 ml, 38.5 mmol) in dichloromethane (10 ml) was added dropwise to the stirred solution and the resulting mixture was maintained at room temperature for 5 hours. The solution was washed with saturated aqueous NaHCO3 (25 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting brown solid was recrystallised (Heptane/EtOAc) to provide the title compound as off-white needles (1.74 g, 63%).

후처리

  1. customExcess reagents were removed in vacuo
  2. additionthe residue was diluted in dichloromethane (50 ml)
  3. additionwas added dropwise to the stirred solution
  4. washThe solution was washed with saturated aqueous NaHCO3 (25 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting brown solid was recrystallised (Heptane/EtOAc)

출처 및 근거

ORD 기록
ord-10ba07166e784d11827685d2f642f38e
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691804B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트