Sodium Bicarbonate → 1-(3-(1H-benzo[d]imidazol-4-yl)phenoxy)-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol

HRID 1399891노트

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HRID 1399891 반응식
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[CH2:11][CH:12]([OH:38])[CH2:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([C:21]2[C:29]3[N:28]=[CH:27][N:26](COCC[Si](C)(C)C)[C:25]=3[CH:24]=[CH:23][CH:22]=2)[CH:16]=1.C([O-])(O)=O.[Na+]>CCO.Cl>[NH:26]1[C:25]2[CH:24]=[CH:23][CH:22]=[C:21]([C:17]3[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=3)[O:14][CH2:13][CH:12]([OH:38])[CH2:11][N:2]3[CH2:3][CH2:4][C:5]4[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=4)[CH2:1]3)[C:29]=2[N:28]=[CH:27]1

참가 물질

5

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온도
80 °C

실험 절차

A mixture of 1-(3,4-dihydroisoquinolin-2(1H)-yl)-3-(3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazol-4-yl)phenoxy)propan-2-ol (265 mg, 0.5 mmol) in EtOH (20 mL) and conc. HCl (1 mL) was stirred at 80° C. overnight. The reaction was adjusted to pH 9 by aq. NaHCO3. The mixture was then extracted with DCM and the combined organic layers dried over Na2SO4 and concentrated to give the crude product. The crude product was purified by pre-HPLC to afford the desired product (50 mg, Yield 25%). 1H NMR (400 MHz, DMSO-d6) δ 8.43 (s, 1H), 8.35 (s, 2H), 7.65 (br.s, 2H), 7.49 (m, 1H), 7.21 (dd, J=7.6 Hz, 1H), 7.12-7.06 (m, 5H), 4.53-4.39 (m, 3H), 4.14 (s, 2H), 2.83-2.57 (m, 6H). LCMS (m/z): 400.1 (M+1).

후처리

  1. extractionThe mixture was then extracted with DCM
  2. dry with materialthe combined organic layers dried over Na2SO4
  3. concentrationconcentrated
  4. customto give the crude product
  5. customThe crude product was purified by pre-HPLC

출처 및 근거

ORD 기록
ord-c96c3b16378448c4aeea56747b3ce87d
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08906900B2

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