Isopropanol → 4-Methyl-benzenesulfinic acid[2-(4-chlorophenyl)-1-cyano-2-methyl-propyl]-amide

HRID 1192384ノート

反応式

HRID 1192384 の反応式
[C-:1]#[N:2].C([Al+]CC)C.C(O)(C)C.[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]([CH3:32])([CH3:31])[CH:20]=[N:21][S@@:22]([C:24]2[CH:29]=[CH:28][C:27]([CH3:30])=[CH:26][CH:25]=2)=[O:23])=[CH:15][CH:14]=1>C1(C)C=CC=CC=1.C1COCC1>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]([CH3:32])([CH3:31])[CH:20]([NH:21][S:22]([C:24]2[CH:25]=[CH:26][C:27]([CH3:30])=[CH:28][CH:29]=2)=[O:23])[C:1]#[N:2])=[CH:15][CH:14]=1

参加物

6

反応物 3

HCID 3776IsopropanolHCID 16686413Diethyl aluminum cyanideHCID 69790886(R)-4-methylbenzenesulfinic acid [2-(4-chlorophenyl)-2-methylpropyliden]-amide

生成物 1

HCID 697909274-Methyl-benzenesulfinic acid[2-(4-chlorophenyl)-1-cyano-2-methyl-propyl]-amide収率 95%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
10 °C

実験手順

The diethyl aluminum cyanide (43.5 mL of a 1.0M solution in toluene, 43.5 mmol) was added to isopropanol (28.9 mL, 377 mmol) and stirred at 10° C. for 15 minutes. This solution was cannulated into the (R)-4-methylbenzenesulfinic acid [2-(4-chlorophenyl)-2-methyl-propylidene]-amide (9.28 g, 29.0 mmol) as a solution in 290 mL of THF at −78° C. This solution was allowed to stir for 15 minutes at −78° C. then allowed to warm slowly to room temperature overnight. The solution was quenched with the addition of diluted NaHCO3 solution and extracted with ethyl acetate. The combined organic was washed with brine, separated, dried over Na2SO4, filtered, and concentrated in vacuo to afford the 4-methyl-benzenesulfinic acid [2-(4-chlorophenyl)-1-cyano-2-methyl-propyl]-amide as a colorless oil (9.55 g, 95% yield). The material was heated to 110° C. (reflux) in concentrated HCl solution over the weekend. The solution was cooled to room temperature, washed with ether, then concentrated in vacuo to give the (S)-2-amino-3-(4-chlorophenyl)-3-methyl-butyric acid hydrochloride salt a white solid (1.61 g, 21%). 1H NMR (DMSO-d6, 400 MHz) δ 8.19 (brs, 1H), 7.48 (d, J=8.0 Hz, 2H), 7.41 (d, J=8.0 Hz, 2H), 7.13 (s, 3H), 4.15 (s, 1H), 1.42 (s, 3H), 1.40 (s, 3H). LCMS (APCI+) m/z 228 [M+H]+; Rt=1.81 min.

後処理

  1. stirringto stir for 15 minutes at −78° C.
  2. temperatureto warm slowly to room temperature overnight
  3. customThe solution was quenched with the addition of diluted NaHCO3 solution
  4. extractionextracted with ethyl acetate
  5. washThe combined organic was washed with brine
  6. customseparated
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-8a13997a036249b7b2241288f096ca69
出典データセット
uspto-grants-2014_03
特許番号
US08680114B2

反応ノート

読み込み中…