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Isopropyl Benzoate → ethyl 3-(1-((2S,3aR,6aR)-3a-((S,4S)-5-(4-(trifluoromethyl)pyridin-2-yl)-2,5-diazabicyclo[2.2.1]heptane-2-carbonyl)octahydropentalen-2-yl)piperidin-4-yl)benzoate

HRID 1400074
ノート
印刷プレビュー

反応式

HRID 1400074 の反応式
[F:1][C:2]([F:28])([F:27])[C:3]1[CH:8]=[CH:7][N:6]=[C:5]([N:9]2[CH2:14][C@@H:13]3[CH2:15][C@H:10]2[CH2:11][N:12]3[C:16]([C@@:18]23[CH2:25][CH2:24][CH2:23][C@@H:22]2[CH2:21][C:20](=O)[CH2:19]3)=[O:17])[CH:4]=1.[NH:29]1[CH2:34][CH2:33][CH:32]([C:35]2[CH:36]=[C:37]([CH:43]=[CH:44][CH:45]=2)[C:38]([O:40][CH2:41][CH3:42])=[O:39])[CH2:31][CH2:30]1.[BH4-].[Na+].C(=O)(O)[O-].[Na+].C(OC(C)C)(=O)C1C=CC=CC=1>ClC(Cl)C.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].CO>[F:28][C:2]([F:27])([F:1])[C:3]1[CH:8]=[CH:7][N:6]=[C:5]([N:9]2[CH2:14][C@@H:13]3[CH2:15][C@H:10]2[CH2:11][N:12]3[C:16]([C@@:18]23[CH2:25][CH2:24][CH2:23][C@@H:22]2[CH2:21][C@H:20]([N:29]2[CH2:34][CH2:33][CH:32]([C:35]4[CH:36]=[C:37]([CH:43]=[CH:44][CH:45]=4)[C:38]([O:40][CH2:41][CH3:42])=[O:39])[CH2:31][CH2:30]2)[CH2:19]3)=[O:17])[CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 13654Isopropyl BenzoateHCID 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 57880398Ethyl 3-(piperidin-4-yl)benzoateHCID 89823414(3aR,6aR)-3a-((1S,4S)-5-(4-(trifluoromethyl)pyridin-2-yl)-2,5-diazabicyclo[2.2.1]heptane-2-carbonyl)hexahydropentalen-2(1H)-one

生成物 1

HCID 86698132
ethyl 3-(1-((2S,3aR,6aR)-3a-((S,4S)-5-(4-(trifluoromethyl)pyridin-2-yl)-2,5-diazabicyclo[2.2.1]heptane-2-carbonyl)octahydropentalen-2-yl)piperidin-4-yl)benzoate

試薬・触媒・溶媒 3

HCID 11026Titanium isopropoxide触媒HCID 887Methanol溶媒HCID 63651,1-Dichloroethane溶媒

実験手順

A mixture of Example 9E (200 mg, 0.5 mmol), ethyl 3-(piperidin-4-yl)benzoate (125 mg, 0.56 mmol) in dichloroethane (20 mL) was added titanium(IV) isopropoxide (0.6 ml, 2.03 mmol) at room temperature. The mixture was stirred at room temperature for 12 hours. Sodium borohydride (96.7 mg, 2.54 mmol) and methanol (1 mL) were added to the reaction mixture and stirred for another 2 hours. LC-MS indicated that the reaction was complete. Aqueous Sodium bicarbonate (20 mL) was added to the reaction mixture. The reaction mixture was extracted with dichloromethane (3×30 mL). The organic fractions were dried with sodium sulfate, filtered, and concentrated. The residue was purified by chromatography (eluent: 20 to 80% ethylacetate in petroleum ether) on silica to give a mixture of the title compound and isopropyl benzoate.

後処理

  1. stirringstirred for another 2 hours
  2. extractionThe reaction mixture was extracted with dichloromethane (3×30 mL)
  3. dry with materialThe organic fractions were dried with sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by chromatography (eluent: 20 to 80% ethylacetate in petroleum ether) on silica
  7. customto give

出典と根拠

ORDレコード
ord-fe7e532311b34cbb8636b2921fb2e7a1
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08906911B2

反応ノート

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