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Acetic Acid → 3-Amino-7-bromoquinoline-2-carboxylic acid

HRID 924371
ノート
印刷プレビュー

反応式

HRID 924371 の反応式
[NH2:1][C:2]1[C:3]([C:13]([O:15]CC)=[O:14])=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([Br:12])[CH:6]=2.O.[OH-].[Li+].C1COCC1.CC(O)=O>O>[NH2:1][C:2]1[C:3]([C:13]([OH:15])=[O:14])=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([Br:12])[CH:6]=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

6

反応物 4

HCID 176Acetic AcidHCID 8028TetrahydrofuranHCID 168937Lithium hydroxide, monohydrateHCID 56965769Ethyl 3-amino-7-bromoquinoline-2-carboxylate

生成物 1

HCID 735548703-Amino-7-bromoquinoline-2-carboxylic acid収率 80.8%

試薬・触媒・溶媒 1

HCID 962Water
溶媒
2 回

反応条件

温度
50 °C

実験手順

To a mixture of ethyl 3-amino-7-bromoquinoline-2-carboxylate (Ark Pharm, 113.9 mg, 0.3859 mmol) and lithium hydroxide monohydrate (82.8 mg, 1.97 mmol), THF (2.50 mL) was added, followed by water (0.50 mL). The resulting mixture was stirred at 50° C. for 2 h. The reaction mixture was then cooled to room temperature and water (25 mL) was then added, followed by AcOH (245.9 mg, 4.095 mmol) to adjust the pH to 5. The mixture was extracted with EtOAc (3×25 mL). The combined organic extract was washed with brine (50 mL), then dried over Na2SO4, and concentrated to yield a yellow solid (83.3 mg). The crude product was used directly in the next step without further purification. LCMS calc. for C10H8BrN2O2(M+H)+: m/z=267.0. found 267.0.

後処理

  1. additionwas added
  2. temperatureThe reaction mixture was then cooled to room temperature
  3. extractionThe mixture was extracted with EtOAc (3×25 mL)
  4. extractionThe combined organic extract
  5. washwas washed with brine (50 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-8a5d4fab190f416587de20e4fb3a380b
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278950B2

反応ノート

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