Ammonium formate → 2-(2-Fluoro-6-chloro-phenyl)-1-morpholin-2-yl-1-phenyl-ethanol hydrochloride

HRID 899105노트

반응식

HRID 899105 반응식
C([N:8]1[CH2:13][CH2:12][O:11][CH:10]([C:14]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([OH:24])[CH2:15][C:16]2[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:23])[CH2:9]1)C1C=CC=CC=1.C([O-])=O.[NH4+]>C(OCC)(=O)C.[Pd]>[ClH:23].[F:22][C:21]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:23])[C:16]=1[CH2:15][C:14]([CH:10]1[O:11][CH2:12][CH2:13][NH:8][CH2:9]1)([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[OH:24]

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 69292291HCID 69292291, 화합물

생성물 1

HCID 692922892-(2-Fluoro-6-chloro-phenyl)-1-morpholin-2-yl-1-phenyl-ethanol hydrochloride수율 74.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 1-(4-Benzyl-morpholin-2-yl)-2-(2-chloro-6-fluoro-phenyl)-1-phenyl-ethanol (450 mg, 1 equiv.) in ethyl acetate (15 mL) at room temperature under nitrogen atmosphere was added ammonium formate (1.69 g, 25 equiv.) followed by addition of palladium on charcoal (10%, 450 g.). The reaction mixture was heated to reflux for 1.5 hours, cooled to room temperature and then filtered through Celite. All volatiles were evaporated under vacuum, and the resulting solid was purified via preparative HPLC. The isolated white solid was taken up in ethanol. Hydrogen chloride was added (large excess of 2M solution in diethyl ether) and the mixture was stirred until it became a clear solution. Then all the volatiles were evaporated “in vacuo”, to give 147 mg of the title compound as white solid. 1H NMR (300 MHz, CD3OD D4) δ: 2.51-2.61 (d, 1H), 2.79-2.91 (t, 1H), 2.96-3.09 (m, 1H), 3.09-3.16 (m, 1H), 3.32-3.54 (q, 2H), 3.82-3.97 (t, 1H), 4.09-4.24 (t, 2H), 6.73-6.84 (t, 1H), 6.93-7.08 (m, 2H), 7.08-7.21 (m, 5H). LCMS (12 minutes method) [M+H]+=336 @ Rt 4.44 min. single major peak.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 1.5 hours
  3. filtrationfiltered through Celite
  4. customAll volatiles were evaporated under vacuum
  5. customthe resulting solid was purified via preparative HPLC
  6. additionHydrogen chloride was added (large excess of 2M solution in diethyl ether)
  7. customThen all the volatiles were evaporated “in vacuo”

출처 및 근거

ORD 기록
ord-cae7fe2d6b9741e1ac6d0677b69d8b2f
출처 데이터셋
uspto-grants-2008_04
특허 번호
US07354920B2

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