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

Cesium carbonate → (3-Fluoro-[2,4]bipyridinyl-3'-yl)-methyl-amine

HRID 878049
노트
인쇄 미리보기

반응식

HRID 878049 반응식
C[N:2]([C:19]1[CH:20]=[N:21][CH:22]=[CH:23][C:24]=1N1CCCCC1C)[C:3](=O)C1C=C(C(F)(F)F)C=C(C(F)(F)F)C=1.[F:32][C:33]1[C:34](B2OC(C)(C)C(C)(C)O2)=[N:35][CH:36]=[CH:37][CH:38]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.[Fe+2].Cl[Cu]>[F:32][C:33]1[C:34]([C:24]2[CH:23]=[CH:22][N:21]=[CH:20][C:19]=2[NH:2][CH3:3])=[N:35][CH:36]=[CH:37][CH:38]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 10796Cesium carbonateHCID 177504653-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 86670691N-Methyl-N-(2-methyl-3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-3'-yl)-3,5-bis-trifluoromethyl-benzamide2회

생성물 1

HCID 68294041(3-Fluoro-[2,4]bipyridinyl-3'-yl)-methyl-amine수율 92.2%

시약·촉매·용매 4

HCID 62652
Cuprous chloride
촉매
HCID 167845palladium(II) acetate촉매
HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)촉매
HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

To a solution of compound (4-bromo-pyridin-3-yl)-methyl-amine (50 mg, 0.267 mmol, example 25, intermediate b) and 3-fluoro pyridine-2-boronic acid pinacol ester (Milestone Pharmtech LLC) (89.4 mg 0.4 mmol) dissolved in dry DMF (3 mL) in a sealed tube was added cesium carbonate (348.4 mg, 1.07 mmol) and the reaction mixture was purged with argon for 10 min. Then Pd(OAc)2 (9.38 mg, 0.013 mmol), dppf (1.48 mg, 0.0026 mmol) and CuCl (26.46 mg, 0.27 mmol) were added to the reaction mixture and again purged with nitrogen for 15 min. The reaction mixture was heated at 100° C. for 16 hours. The reaction mixture was cooled to 25° C., filtered through a bed of celite and washed with EtOAc. The organic layer was washed with water, dried over sodium sulphate and evaporated to yield the desired compound as a light yellow solid (50 mg, 92%) which was used in next step without further purification. MS (ESI): m/z=204.2 [M+H]+.

후처리

  1. customthe reaction mixture was purged with argon for 10 min
  2. customagain purged with nitrogen for 15 min
  3. temperatureThe reaction mixture was cooled to 25° C.
  4. filtrationfiltered through a bed of celite
  5. washwashed with EtOAc
  6. washThe organic layer was washed with water
  7. dry with materialdried over sodium sulphate
  8. customevaporated

출처 및 근거

ORD 기록
ord-14eb9e5da0274903844a74c9025557eb
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08987307B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트