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

Trifluoroacetic acid → HCID 66724616, 화합물

HRID 250068
노트
인쇄 미리보기

반응식

HRID 250068 반응식
COC1C=C(OC)C=CC=1C[NH:6][C:7]1[CH:16]=[N:15][C:14]2[C:9](=[CH:10][C:11]([CH3:17])=[CH:12][CH:13]=2)[N:8]=1.[C:24]([OH:30])([C:26]([F:29])([F:28])[F:27])=[O:25]>C(Cl)Cl>[F:27][C:26]([F:29])([F:28])[C:24]([OH:30])=[O:25].[CH3:17][C:11]1[CH:10]=[C:9]2[C:14]([N:15]=[CH:16][C:7]([NH2:6])=[N:8]2)=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 57476572HCID 57476572, 화합물

생성물 1

HCID 66724616HCID 66724616, 화합물수율 85.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

N-(2,4-Dimethoxybenzyl)-7-methylquinoxalin-2-amine (0.85 g, 2.75 mmol) was stirred in TFA (10 mL, 130 mmol)/CH2Cl2 (10 mL) at room temperature for 30 min. Solvents were removed on the rotary evaporator. Saturated aqueous NaHCO3 (200 mL) was added to the red residue, which then precipitated a pink solid. The mixture was extracted extensively with DCM. The organic layer was dried over sodium sulfate, concentrated, and dried under vacuum to afford 7-methylquinoxalin-2-amine 2,2,2-trifluoroacetate (640 mg, 2.34 mmol, 85% yield).

후처리

  1. customSolvents were removed on the rotary evaporator
  2. additionSaturated aqueous NaHCO3 (200 mL) was added to the red residue, which
  3. customthen precipitated a pink solid
  4. extractionThe mixture was extracted extensively with DCM
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-091ff6f601bc422bbf4b2fd8f1f766b2
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863291B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트