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

Sodium Carbonate → 5-(2-Amino-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N-tert-butylpyridine-3-sulfonamide

HRID 384744
노트
인쇄 미리보기

반응식

HRID 384744 반응식
Br[C:2]1[CH:3]=[C:4]([S:8]([NH:11][C:12]([CH3:15])([CH3:14])[CH3:13])(=[O:10])=[O:9])[CH:5]=[N:6][CH:7]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.C([O-])(=O)C.[K+].Br[C:40]1[CH:41]=[CH:42][C:43]2[N:44]([N:46]=[C:47]([NH2:49])[N:48]=2)[CH:45]=1.C([O-])([O-])=O.[Na+].[Na+]>C(Cl)Cl.CCO.O1CCOCC1>[C:12]([NH:11][S:8]([C:4]1[CH:5]=[N:6][CH:7]=[C:2]([C:40]2[CH:41]=[CH:42][C:43]3[N:44]([N:46]=[C:47]([NH2:49])[N:48]=3)[CH:45]=2)[CH:3]=1)(=[O:10])=[O:9])([CH3:15])([CH3:14])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 10340Sodium CarbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 252159406-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 617949515-Bromo-N-tert-butylpyridine-3-sulfonamide

생성물 1

HCID 426232235-(2-Amino-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N-tert-butylpyridine-3-sulfonamide
수율 184.5%

시약·촉매·용매 3

HCID 702Ethanol용매HCID 6344Dichloromethane용매2회HCID 312751,4-Dioxane용매

반응 조건

온도
120 °C

실험 절차

5-bromo-N-tert-butylpyridine-3-sulfonamide (375 mg, 0.986 mmol), bis(pinacolato) diboron (276 mg, 1.085 mmol), potassium acetate (290 mg, 2.96 mmol), [1,1′bis(diphenylphosphino)ferrocene]dichloro-palladium (II) complex with CH2Cl2 (40 mg, 0.049 mmol) and dioxane (3 ml) were heated to 120° C. for 60 minutes in the microwave. After this time aryl bromide (A) (147 mg, 0.69 mmol), Na2CO3 (2M aqueous solution, 2 mL), EtOH (0.4 ml) and a further portion of [1,1′bis(diphenylphosphino)ferrocene]dichloro-palladium (II) complex with CH2Cl2 was added and reaction mixture heated further for 60 minutes at 120° C. in the microwave. After this time the solvents were removed in vacuo and the brown residue redissolved in 2M HCl (30 mL), the aqueous phase was washed with ethyl acetate (3×20 mL) and then neutralized with concentrated NaOH to pH 7.0. The aqueous phase was then extracted with ethyl acetate (3×20 mL), the organic extracts were combined, dried over sodium sulfate, filtered and the solvent removed in vacuo to afford the desired product as a brown solid (441 mg, 54%).

후처리

  1. customreaction mixture
  2. customAfter this time the solvents were removed in vacuo
  3. dissolutionthe brown residue redissolved in 2M HCl (30 mL)
  4. washthe aqueous phase was washed with ethyl acetate (3×20 mL)
  5. extractionThe aqueous phase was then extracted with ethyl acetate (3×20 mL)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-9d0d2cf4a8984810b5cc3dab931eaac6
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367830B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트