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

Dimethylformamide → HCID 68553177, 화합물

HRID 2382100
노트
인쇄 미리보기

반응식

HRID 2382100 반응식
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1.CC([O-])(C)C.[K+].O(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O.C[N:33](C=O)C>>[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[N:4]([NH2:33])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 90495Di-tert-butyl dicarbonateHCID 213006013-Methyl-1H-pyrrolo[2,3-C]pyridineHCID 23665647Potassium tert-butoxide

생성물 1

HCID 68553177HCID 68553177, 화합물수율 35%

실험 절차

A mixture of 3-methyl-1H-pyrrolo[2,3-c]pyridine (1.21 g, 9.16 mmol), KOtBu (2.05 g, 18.3 mmol) in DMF (41 mL) is purged with N2 and stirred at rt for 2 h. Chloramine in ether (0.15 M, 92 mL) is added and the mixture is stirred for 20 min. The reaction is cooled to 00 C. and a solution of Na2S2O3 (5 g) in water (80 mL) is added. The mixture is stirred for 10 min, and then concentrated in vacuo. The residue is triturated in DCM and filtered. DCM is added, cooled to 0° C. and charged with BOC2O (541 mg, 2.48 mmol). The resulting mixture is separated by silica gel chromatography eluting with 10% MeOH in DCM to afford 3-methyl-pyrrolo[2,3-c]pyridin-1-yl amine (468 mg, 35%). MS: 148 (M+H); 1H NMR (300 MHz, CDCl3): δ 8.85 (s, 1H), 8.27 (d, 1H), 7.46 (d, 1H), 7.09 (s, 1H), 2.30 (s, 3H).

후처리

  1. customis purged with N2
  2. additionChloramine in ether (0.15 M, 92 mL) is added
  3. stirringthe mixture is stirred for 20 min
  4. temperatureThe reaction is cooled to 00 C
  5. additionand a solution of Na2S2O3 (5 g) in water (80 mL) is added
  6. stirringThe mixture is stirred for 10 min
  7. concentrationconcentrated in vacuo
  8. customThe residue is triturated in DCM
  9. filtrationfiltered
  10. additionDCM is added
  11. temperaturecooled to 0° C.
  12. customThe resulting mixture is separated by silica gel chromatography
  13. washeluting with 10% MeOH in DCM

출처 및 근거

ORD 기록
ord-27f12b68a20c4697b651d13d02a9b3b0
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08258130B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트