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3-bromo-N-cyclopropyl-5-nitropyridin-4-amine → 5-Bromo-N~4~-cyclopropylpyridine-3,4-diamine

HRID 1394196
ノート
印刷プレビュー

反応式

HRID 1394196 の反応式
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([N+:12]([O-])=O)[C:7]=1[NH:8][CH:9]1[CH2:11][CH2:10]1>C(O)(=O)C.[Fe]>[Br:1][C:2]1[C:7]([NH:8][CH:9]2[CH2:11][CH2:10]2)=[C:6]([NH2:12])[CH:5]=[N:4][CH:3]=1
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

4

反応物 1

HCID 249036703-bromo-N-cyclopropyl-5-nitropyridin-4-amine

生成物 1

HCID 249036715-Bromo-N~4~-cyclopropylpyridine-3,4-diamine

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

反応条件

温度
80 °C

実験手順

To a stirred solution of the product obtained from Step 3 (2.95 g, 11.4 mmol) in glacial acetic acid (50 ml) was added iron dust (3.35 g, 60 mmol). The resulting mixture was stirred at 80° C. for 90 minutes, after which it was filtered through Celite and the liquor concentrated under vacuum. The crude product was re-dissolved in ethyl acetate, basified with sodium bicarbonate and refiltered. Th organic phase was washed with water three times, followed by twice with brine before concentrating under vacuum to give the product. Passed through a silica plug affording product as an oil, 1.65 g (63%); MS (ES+) m/e 228/230 [M+H]+.

後処理

  1. filtrationafter which it was filtered through Celite
  2. concentrationthe liquor concentrated under vacuum
  3. dissolutionThe crude product was re-dissolved in ethyl acetate
  4. washTh organic phase was washed with water three times
  5. concentrationbefore concentrating under vacuum
  6. customto give the product
  7. customaffording product as an oil, 1.65 g (63%)

出典と根拠

ORDレコード
ord-f2cf3318c4c54641bba99b24e8a05e1c
出典データセット
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07348339B2

反応ノート

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