Hydrochloric Acid → 2-(4-Dimethylaminomethyl-3-fluoro-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one

HRID 2298930

반응식

HRID 2298930 반응식
[F:1][C:2]1[CH:9]=[C:8]([C:10]2[NH:11][C:12]3[CH:13]=[CH:14][CH:15]=[C:16]4[C:22](=[O:23])[NH:21][CH2:20][CH2:19][C:18]=2[C:17]=34)[CH:7]=[CH:6][C:3]=1[CH:4]=O.Br[C:25]1C=CC(C=O)=C(F)C=1.[C:34]([BH3-])#[N:35].[Na+].Cl>CNC.CO.[Cl-].[Zn+2].[Cl-]>[CH3:25][N:35]([CH2:4][C:3]1[CH:6]=[CH:7][C:8]([C:10]2[NH:11][C:12]3[CH:13]=[CH:14][CH:15]=[C:16]4[C:22](=[O:23])[NH:21][CH2:20][CH2:19][C:18]=2[C:17]=34)=[CH:9][C:2]=1[F:1])[CH3:34]

참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 1435174-Bromo-2-fluorobenzaldehydeHCID 5003444Sodium cyanoborohydrideHCID 222666772-Fluoro-4-(6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-2-yl)-benzaldehyde

생성물 1

HCID 222666892-(4-Dimethylaminomethyl-3-fluoro-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one

시약·촉매·용매 3

HCID 3007855Zincchloride촉매HCID 674Dimethylamine용매HCID 887Methanol용매2회

실험 절차

2-Fluoro-4-(6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-2-yl)-benzaldehyde (72 mg, 0.23 mmol. Prepared via the standard two-step, one-pot suzuki coupling of the tricyclic bromide and 4-bromo-2-fluoro-benzaldehyde as described for Example YY) was dissolved in 2 mL 2.0 M dimethylamine in methanol. The orange solution was stirred at room temperature 10 min. The reaction was then cooled to 0° C. and a solution containing zinc chloride (17 mg, 0.13 mmol) and sodium cyanoborohydride (16 mg, 0.26 mmol) in 1 mL methanol, was added dropwise. The pH was adjusted to ca. 3 with concentrated HCl. The reaction was stirred for one hour as the temperature gradually warmed to room temperature. The reaction was partitioned between CHCl3 and water. The pH of the aqueous layer was adjusted to ca. 13 with solid KOH. The layers were separated, and the aqueous layer extracted with 25% iPrOH/CHC13. The combined organic layers were dried (MgSO4) then concentrated in vacuo. Radial chromatography (eluting with 5% MeOH/CHCl3) then crystallization from CH2Cl2/hexanes yielded 2-(4-dimethylaminomethyl-3-fluoro-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 60 mg (76%) as a yellow solid.: m.p. 221.5-222.5° C.; 1H NMR (300 MHz, d6-DMSO) δ2.19 (s, 6H), 3.08 (m, 2H), 3.39 (m, 2H), 3.50 (s, 2H), 7.23 (app t, J=7.8 Hz, 1H), 7.50 (m, 4H), 7.69 (d, J=7.5 Hz, 1H) 8.10 (br t, 1H), 11.62 (br s, 1H). MS (FAB, MH+) 338. Anal. (C20H20FN3O) C, H, N.

후처리

  1. temperatureThe reaction was then cooled to 0° C.
  2. additionwas added dropwise
  3. stirringThe reaction was stirred for one hour as the temperature
  4. temperaturegradually warmed to room temperature
  5. customThe reaction was partitioned between CHCl3 and water
  6. customThe layers were separated
  7. extractionthe aqueous layer extracted with 25% iPrOH/CHC13
  8. dry with materialThe combined organic layers were dried (MgSO4)
  9. concentrationthen concentrated in vacuo
  10. washRadial chromatography (eluting with 5% MeOH/CHCl3)
  11. customcrystallization from CH2Cl2/hexanes

출처 및 근거

ORD 기록
ord-7546f7b31bc04f33b8b0c5ac3fc6efff
출처 데이터셋
uspto-grants-2002_12
특허 번호
US06495541B1

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