Diisopropylamine → HCID 19906419, 화합물

HRID 2371810노트

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HRID 2371810 반응식
C([Li])CCC.C(NC(C)C)(C)C.[F:13][C:14]([F:28])([F:27])[C:15]([NH:17][C:18]1[CH:26]=[C:25]2[C:21]([CH2:22][CH:23]=[CH:24]2)=[CH:20][CH:19]=1)=[O:16].Br[CH2:30][C:31]1[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][C:32]=1[O:41][CH3:42].[Cl-].[NH4+]>CCCCCC.O1CCCC1.C(OCC)(=O)C>[CH3:42][O:41][C:32]1[CH:33]=[C:34]([CH:39]=[CH:40][C:31]=1[CH2:30][C:24]1[C:25]2[C:21](=[CH:20][CH:19]=[C:18]([NH:17][C:15](=[O:16])[C:14]([F:27])([F:28])[F:13])[CH:26]=2)[CH2:22][CH:23]=1)[C:35]([O:37][CH3:38])=[O:36]

참가 물질

9

반응물 5

HCID 7912DiisopropylamineHCID 25517Ammonium ChlorideHCID 2759828Methyl 4-(bromomethyl)-3-methoxybenzoateHCID 19906414HCID 19906414, 화합물HCID 178418339Butyllithium

생성물 1

HCID 19906419HCID 19906419, 화합물수율 14%

시약·촉매·용매 3

HCID 8028Tetrahydrofuran용매3회HCID 8058Hexane용매HCID 8857Ethyl Acetate용매

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온도
-100 °C

실험 절차

A solution of n-butyllithium in hexane (1.4M, 38.82 ml) was added to a -78° C. solution of diisopropylamine (7.85 ml) in tetrahydrofuran (25 ml). After stirring for 15 min, a solution of 6-(trifluoroacetamido)-3H-indene (5.92 g) in tetrahydrofuran (25 ml) was added and stirred for 1 h. The reaction mixture was cooled to -100° C. and a solution of methyl 4-bromomethyl-3-methoxybenzoate (8.44 g) in tetrahydrofuran (35 ml) was added. The mixture was allowed to warm to room temperature and stirred for 18 h. The reaction mixture was added to saturated ammonium chloride (100 ml) and ethyl acetate (150 ml). The mixture was washed (water, brine), dried (MgSO4) and evaporated. The residue was recrystallized from 10:1 methylene chloride:hexane to give methyl 3-methoxy-4-[6-(trifluoroacetamido)-3H-inden-1-ylmethyl]benzoate (1.48 g, 14%). The residue derived from the filtrate was recrystallized from 3:1 methylene chloride:hexane to give a mixture of methyl 3-methoxy-4-[6-(trifluoroacetamido)-3H-inden-1-ylmethyl]benzoate and methyl 3-methoxy-4-[6-(trifluoroacetamido)-1H-inden-1-ylmethyl]benzoate (1.92 g). This mixture was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (1.11 g) and tetrahydrofuran (20 ml) for 18 h. After partitioning between ethyl acetate (85 ml) and 1N hydrochloric acid, the organic layer was washed (brine) and dried (MgSO4). Evaporation and trituration with methylene chloride gave a colorless solid. This was combined with the above material to give methyl 3-methoxy-4-[6-(trifluoroacetamido)-3H-inden-1-ylmethyl]-3-methoxybenzoate (2.81 g, 27% total yield from 6-(trifluoroacetamido)-3H-indene); mp 198.5°-200.0° C.; MS(CI), m/e=406(M+H).

후처리

  1. stirringstirred for 1 h
  2. temperatureto warm to room temperature
  3. stirringstirred for 18 h
  4. washThe mixture was washed (water, brine)
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue was recrystallized from 10:1 methylene chloride

출처 및 근거

ORD 기록
ord-56667ed56ffb426d8ad66674b71efdc8
출처 데이터셋
uspto-grants-1992_03
특허 번호
US05095038

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