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Hydrochloric Acid → HCID 178468175、化合物

HRID 1047365
ノート
印刷プレビュー

反応式

HRID 1047365 の反応式
[CH:1](NC(C)C)(C)C.C([Li])CCC.[N+:13]([C:16]1[CH:21]=[CH:20][C:19]([NH:22][C@H:23]2[CH2:28][CH2:27][C@H:26]([O:29][CH2:30][C:31]([N:33]3[CH2:38][CH2:37][N:36]([C:39]4[CH:44]=[CH:43][C:42]([C:45]([F:48])([F:47])[F:46])=[CH:41][CH:40]=4)[CH2:35][CH2:34]3)=[O:32])[CH2:25][CH2:24]2)=[CH:18][C:17]=1[C:49]([F:52])([F:51])[F:50])([O-:15])=[O:14].C([N-]C(C)C)(C)C.[Li+].CI.[Cl-].[NH4+].Cl>O1CCCC1>[N+:13]([C:16]1[CH:21]=[CH:20][C:19]([NH:22][C@H:23]2[CH2:28][CH2:27][C@H:26]([O:29][CH:30]([CH3:1])[C:31]([N:33]3[CH2:34][CH2:35][N:36]([C:39]4[CH:44]=[CH:43][C:42]([C:45]([F:46])([F:47])[F:48])=[CH:41][CH:40]=4)[CH2:37][CH2:38]3)=[O:32])[CH2:25][CH2:24]2)=[CH:18][C:17]=1[C:49]([F:52])([F:51])[F:50])([O-:15])=[O:14]
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

9

反応物 7

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 7912DiisopropylamineHCID 25517Ammonium ChlorideHCID 2724682Lithium diisopropylamideHCID 178418339ButyllithiumHCID 178521456HCID 178521456、化合物

生成物 1

HCID 178468175HCID 178468175、化合物収率 52%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-35 °C

実験手順

To a solution of diisopropylamine (0.28 mL, 2.0 mmol) in dry tetrahydrofuran (3 mL) at 5° C. was added n-butyllithium (2.5 M solution in hexanes, 1 mL, 2.5 mmol). The resulting mixture was allowed to stir for 30 min. Meanwhile, 2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-1-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-ethanone (287 mg, 0.5 mmol, prepared in accordance with Example 11) was dissolved in dry tetrahydrofuran (2 mL). The solution was then cooled to −35° C. To the cooled solution was added an aliquot from the freshly prepared lithium diisopropylamide solution (1.8 mL). Stirring was continued for another 30 min. Methyliodide (37 μL, 0.6 mmol) was then added, and the mixture was allowed to attain −10° C. over 1 hr. Saturated ammonium chloride solution was then added (3 mL), and the mixture warmed to room temperature and acidified to a pH of 3 with 1 N HCl. The aqueous solution was then extracted with ethyl acetate (2×15 mL), and the combined organic layers were washed with brine (2×5 mL), dried over magnesium sulfate, and concentrated. Purification by column chromatography (Ethyl acetate/cyclohexanes, 4:1) afforded the desired product as an orange solid (152 mg, 52% yield). The structure was confirmed using Protocol I-B. Calculated mass=589; observed mass=589; HPLC retention time=5.82 min.

後処理

  1. stirringStirring
  2. waitwas continued for another 30 min
  3. waitto attain −10° C. over 1 hr
  4. temperaturethe mixture warmed to room temperature
  5. extractionThe aqueous solution was then extracted with ethyl acetate (2×15 mL)
  6. washthe combined organic layers were washed with brine (2×5 mL)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. customPurification by column chromatography (Ethyl acetate/cyclohexanes, 4:1)

出典と根拠

ORDレコード
ord-3f6913fbaecf423fa46f595089687c17
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569495B2

反応ノート

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