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Dimethylformamide → Methyl 4-hydroxy-3-iodobenzoate

HRID 1714577
ノート
印刷プレビュー

反応式

HRID 1714577 の反応式
CC(OC(N[C@@H:9](CC1C=CC(C2N=C(C(N(C)OC)=O)N(C)C=2)=CC=1)[CH2:10][CH2:11][C:12]([O:14][C:15](C)(C)C)=[O:13])=O)(C)C.[I:38][CH:39]([CH3:41])[CH3:40].CCN(C(C)C)C(C)C.CN(C=[O:55])C>>[OH:55][C:40]1[CH:9]=[CH:10][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:41][C:39]=1[I:38]
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 4

HCID 6228DimethylformamideHCID 6362Isopropyl iodideHCID 81531DiisopropylethylamineHCID 866047661,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl)amino)-5-[4-(1-methyl-2-{[methyl(methyloxy)amino]carbonyl}-1H-imidazol-4-yl)phenyl]pentanoate

生成物 1

HCID 11346465Methyl 4-hydroxy-3-iodobenzoate収率 20%

反応条件

温度
80 °C

実験手順

To a solution of compound 1 (200 mg, 1.077 mmol) and 2-iodopropane, (322 uL, 3.23 mmol) in DMF (10 mL) was added DIEA (750 uL, 4.31 mmol). The reaction mixture was heated to 80° C. and stirred overnight. The reaction was monitored by LC/MS. After the reaction was done it was cooled to room temperature. The reaction mixture was quenched with HCl (0.5 N, 30 mL) and extracted with ethyl acetate (50 mL×3). The organic layer was dried over sodium sulfate and concentrated and dried under high vacuum. The resulting residue was purified by reverse phase chromatography using a mixture of acetonitrile and water to give compound 2 (50 mg, 20%).

後処理

  1. temperaturewas cooled to room temperature
  2. customThe reaction mixture was quenched with HCl (0.5 N, 30 mL)
  3. extractionextracted with ethyl acetate (50 mL×3)
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. concentrationconcentrated
  6. customdried under high vacuum
  7. customThe resulting residue was purified by reverse phase chromatography
  8. additiona mixture of acetonitrile and water

出典と根拠

ORDレコード
ord-e2e4cc66bc86493ba08e952ba9ad5ca2
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07795448B2

反応ノート

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