Potassium hydride → N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine

HRID 1734688노트

반응식

HRID 1734688 반응식
[C:1]([NH:20][CH:21]([CH2:40][OH:41])[CH2:22][O:23][CH2:24][C:25]1[CH:30]=[CH:29][C:28]([C:31]2[O:32][C:33]3[CH:39]=[CH:38][CH:37]=[CH:36][C:34]=3[N:35]=2)=[CH:27][CH:26]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[K+].[C:44]1([CH2:50][CH2:51][CH2:52][CH2:53]I)[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1>C1COCC1>[C:1]([NH:20][CH:21]([CH2:40][O:41][CH2:53][CH2:52][CH2:51][CH2:50][C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)[CH2:22][O:23][CH2:24][C:25]1[CH:26]=[CH:27][C:28]([C:31]2[O:32][C:33]3[CH:39]=[CH:38][CH:37]=[CH:36][C:34]=3[N:35]=2)=[CH:29][CH:30]=1)([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

참가 물질

5

반응물 3

HCID 82127Potassium hydrideHCID 12709818(4-Iodobutyl)benzeneHCID 19420787N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-hydroxy-2-propanamine

생성물 1

HCID 19420792N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
20 °C

실험 절차

N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-hydroxy-2-propanamine (0.4 g; 0.74 mmol) is added to a suspension of potassium hydride (0.12 g; 1. mmol; 35% suspension in oil) in dry THF (4 ml) at 0° C. The reaction is stirred for 15 minutes at 20° C. 4-Phenyl-1-butyl iodide (0.21 g; 0.81 mmol) is added and the reaction mixture stirred for 15 hours. The reaction is quenched with MeOH, diluted with CH2Cl2 and washed with water 2x. The organic phase is dried (Na2SO4), concentrated and purified by column chromatography with 80% CH2Cl2 /20% petroleum ether to yield N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine as an oil which is used directly in Step F.

후처리

  1. stirringthe reaction mixture stirred for 15 hours
  2. customThe reaction is quenched with MeOH
  3. additiondiluted with CH2Cl2
  4. washwashed with water 2x
  5. dry with materialThe organic phase is dried (Na2SO4)
  6. concentrationconcentrated
  7. custompurified by column chromatography with 80% CH2Cl2 /20% petroleum ether

출처 및 근거

ORD 기록
ord-3800d536b0764b818291d1eb14bacd76
출처 데이터셋
uspto-grants-1996_07
특허 번호
US05534532

반응 노트

불러오는 중…