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Methanol → (R)-2-Amino-5,5,5-trifluoropentanamide hydrochloride

HRID 1803729
ノート
印刷プレビュー

反応式

HRID 1803729 の反応式
[ClH:1].[F:2][C:3]([F:20])([F:19])[CH2:4][CH2:5][C@@H:6]([NH:10][C@@H](C1C=CC=CC=1)C)[C:7]([NH2:9])=[O:8].CO.O>[Pd].[OH-].[OH-].[Pd+2].ClCCl>[ClH:1].[NH2:10][C@H:6]([CH2:5][CH2:4][C:3]([F:2])([F:19])[F:20])[C:7]([NH2:9])=[O:8]
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 3

HCID 887MethanolHCID 962WaterHCID 66649708(R)-5,5,5-trifluoro-2-(((R)-1-phenylethyl)amino)pentanamide hydrochloride

生成物 1

HCID 70700839(R)-2-Amino-5,5,5-trifluoropentanamide hydrochloride収率 91.8%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 9942167
Palladium hydroxide
触媒
HCID 6344Dichloromethane溶媒

反応条件

温度
32.5 °C

実験手順

To a suitable pressure vessel, (R)-5,5,5-trifluoro-2-((R)-1-phenylethylamino)-pentanamide hydrochloride (1.50 kg) was charged along with methanol (15.0 L). This was followed by the addition of water (701.0 mL) followed by 20% palladium hydroxide on carbon (225 g). Similarly, palladium on carbon (Pd/C) could be used as the hydrogenation catalyst. The vessel was flushed with nitrogen three times, and then hydrogen gas was pressurized into the vessel (3-4 kg/cm2) at 60° C. The reaction was monitored for completion by HPLC. Upon completion, the reaction mixture was allowed to cool to 30-35° C. and filtered through a Celite pad, then washed with methanol. The filtrate was then concentrated under reduced pressure. After complete concentration, the remaining reaction mixture was treated with dichloromethane (2.5 L per wash), filtered and dried at 45° C. for 12 hours, giving the title compound (915 g, 91.0%; Purity=97%). 1H NMR (DMSO-d6) (400 MHz) δ 2.00 (m, 2H, CH2), 2.30-2.40 (m, 211 of CH2—CF3), 3.85-3.88 (m, 1H, —(CONH2)CH(NH), 7.64 & 8.11 (br s, 1H, each of CONH2), 8.44 (br s, 311, 13C NMR (DMSO-d6) (100.0 MHz) δ 169.57, 131.20, 128.45, 125.71, 122.97, 50.91, 29.46, 29.18, 28.89, 28.61, 23.56, 23.53.

後処理

  1. customThe vessel was flushed with nitrogen three times
  2. customwas pressurized into the vessel (3-4 kg/cm2) at 60° C
  3. filtrationfiltered through a Celite pad
  4. washwashed with methanol
  5. concentrationThe filtrate was then concentrated under reduced pressure
  6. concentrationAfter complete concentration
  7. customthe remaining reaction mixture
  8. filtrationfiltered
  9. customdried at 45° C. for 12 hours

出典と根拠

ORDレコード
ord-dc319fabd45d4912a7d470affa0ef5f2
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08350084B2

反応ノート

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