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Ammonium Chloride → HCID 22638594、化合物

HRID 2416199
ノート
印刷プレビュー

反応式

HRID 2416199 の反応式
[CH2:1]([C:3]1[CH:8]=[C:7]([C:9]2[S:10][CH:11]=[C:12]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[N:13]=2)[CH:6]=[CH:5][N:4]=1)[CH3:2].[F:19][C:20]1[CH:21]=[CH:22][C:23]([N+:28]([O-:30])=[O:29])=[C:24]([CH:27]=1)[CH2:25]Br.[NH4+].[Cl-]>C1(C)C=CC=CC=1>[CH2:1]([C:3]1[CH:8]=[C:7]([C:9]2[S:10][CH:11]=[C:12]([CH:14]([CH2:25][C:24]3[CH:27]=[C:20]([F:19])[CH:21]=[CH:22][C:23]=3[N+:28]([O-:30])=[O:29])[C:15]([O:17][CH3:18])=[O:16])[N:13]=2)[CH:6]=[CH:5][N:4]=1)[CH3:2]
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

5

反応物 3

HCID 25517Ammonium ChlorideHCID 105616432-(Bromomethyl)-4-fluoro-1-nitrobenzeneHCID 22638557HCID 22638557、化合物

生成物 1

HCID 22638594HCID 22638594、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
-78 °C

実験手順

Methyl 2-[2-(2-ethyl-4-pyridyl)-1,3-thiazole-4-yl]acetate (520 mg, 2.0 mmol) (Example 12(a)) was dissolved in toluene and the solution was concentrated by rotary evaporation. This procedure was repeated, and the dry residue was dissolved in 18 mL anhydrous THF (18 mL). The solution was cooled to −78° C., and LHMDS (2.1 mL, 1.0 M in THF, Aldrich) was added slowly via a syringe. To the resulting red solution, 5-fluoro-2-nitrobenzyl bromide (400 mg, 1.7 mmol) was added as a solid in one portion. The reaction was warmed slowly to RT over 4 h. Saturated aqueous NH4Cl (50 mL) was added, and the mixture was extracted with 100 mL of EtOAc. The organic layer was separated, washed with H2O (100 mL), dried (Na2SO4), and concentrated. Flash chromatography (gradient elution: 10-40% EtOAc in hexanes) of the crude material afforded the title compound as a clear oil. MS m/z: 416 (M+1). Calc'd for C20H18FN3O4S: 415.10.

後処理

  1. concentrationthe solution was concentrated by rotary evaporation
  2. dissolutionthe dry residue was dissolved in 18 mL anhydrous THF (18 mL)
  3. additionLHMDS (2.1 mL, 1.0 M in THF, Aldrich) was added slowly via a syringe
  4. temperatureThe reaction was warmed slowly to RT over 4 h
  5. extractionthe mixture was extracted with 100 mL of EtOAc
  6. customThe organic layer was separated
  7. washwashed with H2O (100 mL)
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated
  10. washFlash chromatography (gradient elution: 10-40% EtOAc in hexanes) of the crude material

出典と根拠

ORDレコード
ord-10339fde41cc4c6f83a37241ddc84bae
出典データセット
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06822097B1

反応ノート

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