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

HRID 1394196
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HRID 1394196 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

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

생성물 1

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

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

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온도
80 °C

실험 절차

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]+.

후처리

  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%)

출처 및 근거

ORD 기록
ord-f2cf3318c4c54641bba99b24e8a05e1c
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07348339B2

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