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

Potassium Carbonate → Pyrazolo[4,3-h]quinazoline-3-carboxamide, 35

HRID 44634
노트
인쇄 미리보기

반응식

HRID 44634 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]2[CH:10]=[C:11]([NH2:15])[CH:12]=[CH:13][CH:14]=2)[CH2:4][CH2:3]1.[CH3:16][NH:17][C:18]([C:20]1[C:24]2[C:25]([CH3:37])([CH3:36])[CH:26](CC)[C:27]3[CH:28]=[N:29][C:30](I)=[N:31][C:32]=3[C:23]=2[N:22]([CH3:38])[N:21]=1)=[O:19].C([O-])([O-])=O.[K+].[K+]>CC([O-])=O.CC([O-])=O.[Pd+2].CN(C)C=O>[CH3:16][NH:17][C:18]([C:20]1[C:24]2[C:25]([CH3:36])([CH3:37])[CH2:26][C:27]3[CH:28]=[N:29][C:30]([NH:15][C:11]4[CH:12]=[CH:13][CH:14]=[C:9]([CH2:8][N:5]5[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]5)[CH:10]=4)=[N:31][C:32]=3[C:23]=2[N:22]([CH3:38])[N:21]=1)=[O:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 64841863-[(4-Methylpiperazin-1-yl)methyl]anilineHCID 86630222ethyl 8-iodo-1,4,4-trimethyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acid methylamide

생성물 1

HCID 44236110Pyrazolo[4,3-h]quinazoline-3-carboxamide, 35수율 62.2%

시약·촉매·용매 2

HCID 167845
palladium(II) acetate
촉매
HCID 6228Dimethylformamide용매2회

반응 조건

온도
80 °C

실험 절차

Pd(OAc)2 (16.34 mg, 0.0728 mmol), (±)-BINAP (45.33 mg, 0.0728 mmol) and dimethylformamide (12 mL) were charged in a round-bottom flask flushed with argon. The mixture was stirred under argon for 30 minutes. Then 3-(4-methyl-piperazin-1-ylmethyl)-phenylamine (448.4 mg, 2.184 mmol), ethyl 8-iodo-1,4,4-trimethyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acid methylamide (300 mg, 0.728 mmol), K2CO3 (1.508 g, 10.910 mmol) and dimethylformamide (10 mL) were added. The resulting mixture was heated to 80° C. in an oil bath under argon with good stirring for 3 hours. After cooling to room temperature, the reaction mixture was filtered by suction filtration washing with dichloromethane and the filtrate was evaporated to dryness. The crude was purified by flash chromatography on silica gel (eluant; dichloromethane/methanol 95:5) to afford 215 mg (yield 62%) of pure title compound.

후처리

  1. customflushed with argon
  2. stirringwith good stirring for 3 hours
  3. temperatureAfter cooling to room temperature
  4. filtrationthe reaction mixture was filtered by suction filtration
  5. washwashing with dichloromethane
  6. customthe filtrate was evaporated to dryness
  7. customThe crude was purified by flash chromatography on silica gel (eluant; dichloromethane/methanol 95:5)

출처 및 근거

ORD 기록
ord-46b6f899c1b346f6859ceac5aeae3666
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541429B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트