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N-bromobutanimide → HCID 86616282, 화합물

HRID 2240131
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HRID 2240131 반응식
[Cl:1][C:2]1[N:3]=[C:4]([CH2:11][CH2:12][CH2:13][NH2:14])[C:5]2[S:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[Br:15]N1C(=O)CCC1=O>C(#N)C>[Br:15][C:8]1[C:6]2[N:7]=[C:2]([Cl:1])[N:3]=[C:4]([CH2:11][CH2:12][CH2:13][NH2:14])[C:5]=2[S:10][CH:9]=1
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 86616281(2-Chlorothieno[3,2-d]pyrimidin-4-yl)propylamine

생성물 1

HCID 86616282HCID 86616282, 화합물수율 64.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
50 °C

실험 절차

8.34 g (36.63 mmol) of (2-chlorothieno[3,2-d]pyrimidin-4-yl)propylamine (IV) is dissolved in 60 mL of acetonitrile and 7.89 g (44.32 mmol) of N-bromosuccinimide is added. The reaction mixture is stirred for 16 hours at ambient temperature and for 6 hours at 50° C. Then it is concentrated by evaporation and the residue is combined with water. The precipitate formed is suction filtered, washed, and dried. 7.25 g of product V (61%) is obtained as a powder.

후처리

  1. concentrationThen it is concentrated by evaporation
  2. customThe precipitate formed
  3. filtrationfiltered
  4. washwashed
  5. customdried

출처 및 근거

ORD 기록
ord-063e8fde9b2648b78c0aa2dbd7be305f
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723341B2

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