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Morpholine → 4-(3-Fluorobenzyl)-N-(2-(5-morpholino-1H-indol-3-yl)ethyl)benzamide

HRID 1777681
ノート
印刷プレビュー

反応式

HRID 1777681 の反応式
C1(P(C2CCCCC2)C2C=CC=CC=2C2C(N(C)C)=CC=CC=2)CCCCC1.CC([O-])(C)C.[Na+].[NH:35]1[CH2:40][CH2:39][O:38][CH2:37][CH2:36]1.Br[C:42]1[CH:43]=[C:44]2[C:48](=[CH:49][CH:50]=1)[NH:47][CH:46]=[C:45]2[CH2:51][CH2:52][NH:53][C:54](=[O:69])[C:55]1[CH:60]=[CH:59][C:58]([CH2:61][C:62]2[CH:67]=[CH:66][CH:65]=[C:64]([F:68])[CH:63]=2)=[CH:57][CH:56]=1>O1CCOCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:68][C:64]1[CH:63]=[C:62]([CH:67]=[CH:66][CH:65]=1)[CH2:61][C:58]1[CH:57]=[CH:56][C:55]([C:54]([NH:53][CH2:52][CH2:51][C:45]2[C:44]3[C:48](=[CH:49][CH:50]=[C:42]([N:35]4[CH2:40][CH2:39][O:38][CH2:37][CH2:36]4)[CH:43]=3)[NH:47][CH:46]=2)=[O:69])=[CH:60][CH:59]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8083MorpholineHCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 23676156Sodium t-butoxideHCID 86699393HCID 86699393、化合物

生成物 1

HCID 679741904-(3-Fluorobenzyl)-N-(2-(5-morpholino-1H-indol-3-yl)ethyl)benzamide収率 6.4%

試薬・触媒・溶媒 2

HCID 167845
palladium(II) acetate
触媒
HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
100 °C

実験手順

A mixture of palladium acetate (0.004 g; 0.017 mmol) and 2′-(dicyclohexylphosphino)-N,N-dimethylbiphenyl-2-amine (0.028 g; 0.071 mmol) in dioxane (0.5 mL) was degassed and sonicated for 30 minutes. This solution was then added to a degassed mixture of sodium 2-methylpropan-2-olate (0.024 g; 0.248 mmol), morpholine (0.031 mL; 0.354 mmol) and N-(2-(5-bromo-1H-indol-3-yl)ethyl)-4-(3-fluorobenzyl)benzamide (0.080 g; 0.177 mmol) in dioxane (2 mL). The resulting mixture was stirred at 100° C. for 18 hours and evaporated to dryness. The residue was partitioned between water and ethyl acetate and the organic layer was dried and concentrated under reduced pressure. The crude material was purified twice by flash chromatography on silica gel (eluent 65 to 100% ethyl acetate in heptane and 20 to 100% ethyl acetate in dichloromethane) and by preparative HPLC (method 2) to afford 0.0052 g (6%) of the title compound as a white solid.

後処理

  1. customwas degassed
  2. customsonicated for 30 minutes
  3. customevaporated to dryness
  4. customThe residue was partitioned between water and ethyl acetate
  5. customthe organic layer was dried
  6. concentrationconcentrated under reduced pressure
  7. customThe crude material was purified twice by flash chromatography on silica gel (eluent 65 to 100% ethyl acetate in heptane and 20 to 100% ethyl acetate in dichloromethane) and by preparative HPLC (method 2)

出典と根拠

ORDレコード
ord-8144a93adc7045fdafee546652036d8e
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09266832B2

反応ノート

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