Proton sponge → 6,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro 1H-benz[e]isoindole hydrochloride

HRID 233413

반응식

HRID 233413 반응식
C([N:8]1[CH2:16][C:15]2[C:14]3[CH:17]=[CH:18][C:19]([O:23][CH3:24])=[C:20]([O:21][CH3:22])[C:13]=3[CH2:12][CH:11]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:10]=2[CH2:9]1)C1C=CC=CC=1.CN(C)C1C2C(=CC=CC=2N(C)C)C=CC=1.[Cl:47]C(OC(Cl)C)=O>ClCCCl>[ClH:47].[CH3:22][O:21][C:20]1[C:13]2[CH2:12][CH:11]([C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:10]3[CH2:9][NH:8][CH2:16][C:15]=3[C:14]=2[CH:17]=[CH:18][C:19]=1[O:23][CH3:24]

참가 물질

5

반응물 3

HCID 88675Proton spongeHCID 5213051-Chloroethyl chloroformateHCID 199611422-benzyl-6,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro-1H-benz[e]isoindole

생성물 1

HCID 199610916,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro 1H-benz[e]isoindole hydrochloride수율 75%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

To a solution of 1.0 g (2.52 mmol) of 2-benzyl-6,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro-1H-benz[e]isoindole, from Step 5, in 22 mL of 1,2-dichloroethane was added 0.11 g (0.05 mmol) of 1,8-bis(dimethylamino)-naphthalene and 0.33 mL (3.15 mmol) of 1-chloroethyl chloroformate at 0° C. The solution was heated to reflux for 2 h and the solvent removed in vacuo. The residue was filtered through silica gel eluted with 25% ethyl acetate in hexanes. After concentration under reduced pressure, methanol (20 mL) was added and the solution was heated to reflux for 30 minutes, before the solvent was removed in vacuo. The product was crystallized from ethanol/ether to give 0.46 g. (75% yield) of 6,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro-1H-benz[e]isoindole hydrochloride as a white solid.; MS DCI: 308 (M+H)+ ; 1H NMR (d6 -DMSO) δ:3.05-3.25 (m, 2H), 3.55 (s, 3H), 3.80 (s, 3H), 3.88 (m, 1H), 4.0-4.15 (m, 2H), 4.25-4.45 (m, 2H), 6.91 (m, 1H), 7.15-7.3 (m, 3H), 7.4-7.6 (m, 3H).

후처리

  1. temperatureThe solution was heated
  2. temperatureto reflux for 2 h
  3. customthe solvent removed in vacuo
  4. filtrationThe residue was filtered through silica gel
  5. washeluted with 25% ethyl acetate in hexanes
  6. concentrationAfter concentration under reduced pressure, methanol (20 mL)
  7. additionwas added
  8. temperaturethe solution was heated
  9. temperatureto reflux for 30 minutes, before the solvent
  10. customwas removed in vacuo
  11. customThe product was crystallized from ethanol/ether
  12. customto give 0.46 g

출처 및 근거

ORD 기록
ord-855c7be2af534f0baa8c0512cbabbd95
출처 데이터셋
uspto-grants-1997_01
특허 번호
US05591884

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