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Lithium Hydroxide → 7-[(5,7-Difluorochroman-4-yl)oxy]-2-methyl-1H-benzo[d]imidazole-5-carboxylic Acid

HRID 2239316
ノート
印刷プレビュー

反応式

HRID 2239316 の反応式
[OH:1][C:2]1[C:10]2[N:9]=[C:8]([CH3:11])[N:7](C(OC(C)(C)C)=O)[C:6]=2[CH:5]=[C:4]([C:19]([O:21]C)=[O:20])[CH:3]=1.[F:23][C:24]1[CH:33]=[C:32]([F:34])[CH:31]=[C:30]2[C:25]=1[CH:26](O)[CH2:27][CH2:28][O:29]2.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.[OH-].[Li+]>C1(C)C=CC=CC=1.O1CCCC1>[F:23][C:24]1[CH:33]=[C:32]([F:34])[CH:31]=[C:30]2[C:25]=1[CH:26]([O:1][C:2]1[C:10]3[N:9]=[C:8]([CH3:11])[NH:7][C:6]=3[CH:5]=[C:4]([C:19]([OH:21])=[O:20])[CH:3]=1)[CH2:27][CH2:28][O:29]2
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 3939Lithium HydroxideHCID 11776TriphenylphosphineHCID 75555Diisopropyl diazene-1,2-dicarboxylateHCID 534275145,7-Difluorochroman-4-olHCID 68577057Methyl 1-Boc-4-hydroxy-2-methyl-1H-benzo[d]imidazole-6-carboxylate

生成物 1

HCID 68574559
7-[(5,7-Difluorochroman-4-yl)oxy]-2-methyl-1H-benzo[d]imidazole-5-carboxylic Acid
収率 73.5%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred mixture of 1-(1,1-dimethylethyl) 6-methyl 4-hydroxy-2-methyl-1H-benzimidazole-1,6-dicarboxylate (1.33 g, 4.34 mmol, STEP 3 in Example 4), (+)-5,7-difluoro-3,4-dihydro-2H-chromen-4-ol (1.82 g, 9.79 mmol, STEP 8 in Example 2) and triphenylphosphine (2.28 g, 8.69 mmol) in toluene (50 mL) was added diisopropyl azodicarboxylate (DIAD) (1.76 g, 8.70 mmol) at room temperature. The reaction mixture was stirred at room temperature for 30 minutes and concentrated in vacuum. The residue was dissolved in methanol (20 mL) and tetrahydrofuran (5 mL), and to the mixture was added 4M lithium hydroxide aqueous solution (18.0 mL, 90.0 mmol) at room temperature. After stirring for 1 hour at 80° C., the reaction mixture was concentrated in vacuum. The residue was dissolved with water (200 mL), acidified with 2M hydrochloric acid aqueous solution (50 mL), and extracted with ethyl acetate (200 mL×3). The organic layers were combined, dried over magnesium sulfate and concentrated in vacuum. The residue was purified by column chromatography on silica gel (gradient elution from ethyl acetate only to ethyl acetate:methanol with 1 wt % of acetic acid=3:1) to afford the title compound as a white solid (1.15 g, 73%, >99% ee).

後処理

  1. concentrationconcentrated in vacuum
  2. dissolutionThe residue was dissolved in methanol (20 mL)
  3. stirringAfter stirring for 1 hour at 80° C.
  4. concentrationthe reaction mixture was concentrated in vacuum
  5. dissolutionThe residue was dissolved with water (200 mL)
  6. extractionextracted with ethyl acetate (200 mL×3)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated in vacuum
  9. customThe residue was purified by column chromatography on silica gel (
  10. washgradient elution from ethyl acetate only to ethyl acetate

出典と根拠

ORDレコード
ord-b6d672bccec24864aaf1e364cbfbf7e6
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723321B2

反応ノート

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