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

3-Aminopyridine → 5-[2-(Pyridin-3-ylamino)-pyrimidin-4-yl]-thiophene-2-carboxylic acid ethyl ester

HRID 1716400
노트
인쇄 미리보기

반응식

HRID 1716400 반응식
CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C(=O)([O-])[O-].[K+].[K+].[CH2:49]([O:51][C:52]([C:54]1[S:55][C:56]([C:59]2[CH:64]=[CH:63][N:62]=[C:61](Cl)[N:60]=2)=[CH:57][CH:58]=1)=[O:53])[CH3:50].[NH2:66][C:67]1[CH:68]=[N:69][CH:70]=[CH:71][CH:72]=1>O1CCOCC1.CCOC(C)=O.O.CC(O)=O.CC(O)=O.[Pd]>[CH2:49]([O:51][C:52]([C:54]1[S:55][C:56]([C:59]2[CH:64]=[CH:63][N:62]=[C:61]([NH:66][C:67]3[CH:68]=[N:69][CH:70]=[CH:71][CH:72]=3)[N:60]=2)=[CH:57][CH:58]=1)=[O:53])[CH3:50]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 4

HCID 100093-AminopyridineHCID 11430Potassium CarbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 594684545-(2-Chloro-pyrimidin-4-yl)-thiophene-2-carboxylic acid ethyl ester

생성물 1

HCID 594686225-[2-(Pyridin-3-ylamino)-pyrimidin-4-yl]-thiophene-2-carboxylic acid ethyl ester수율 62.4%

시약·촉매·용매 4

HCID 4144353Palladium (II) acetate촉매HCID 962Water용매HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매2회

반응 조건

온도
100 °C

실험 절차

Palladium II acetate (8.3 mg, 0.1 mmol) and xantphos 42.8 mg, 0.2 mmol) were precombined in 4 mL dry dioxane under nitrogen gas. Potassium carbonate (1.03 g, 7.46 mmol) was added followed by a solution of 5-(2-Chloro-pyrimidin-4-yl)-thiophene-2-carboxylic acid ethyl ester (100 mg, 0.373 mmol) and 3-aminopyridine (42 mg, 0.447 mmol) in 3 mL dioxane. The reaction was heated in a capped vial at 100° C. for 20 h. The cooled reaction mixture was diluted with EtOAc and water and the layers were separated. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was redissolved in ethyl ether and treated with 2 M HCl in ether to generate a precipitate which was collected by filtration to afford 76 mg (56.3%) of the title compound. The crude material was used in the next step.

후처리

  1. customThe cooled reaction mixture
  2. customthe layers were separated
  3. dry with materialThe organic layer was dried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was redissolved in ethyl ether
  6. additiontreated with 2 M HCl in ether
  7. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-bf900d67e68c423eb983bb4e43a66734
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07803806B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트