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N-bromobutanimide → 6-Bromo-5-chloro-1,2,3,4-tetrahydro-1,8-naphthyridine

HRID 712772
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반응식

HRID 712772 반응식
[Cl:1][C:2]1[CH:11]=[CH:10][N:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][NH:7]2.[Br:12]N1C(=O)CCC1=O>C(Cl)Cl>[Br:12][C:11]1[C:2]([Cl:1])=[C:3]2[C:8](=[N:9][CH:10]=1)[NH:7][CH2:6][CH2:5][CH2:4]2
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 585167685-Chloro-1,2,3,4-tetrahydro-1,8-naphthyridine

생성물 1

HCID 1176677456-Bromo-5-chloro-1,2,3,4-tetrahydro-1,8-naphthyridine수율 91.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 5-chloro-1,2,3,4-tetrahydro-[1,8]naphthyridine (500 mg, 3.0 mmol) in DCM (40 mL) is added N-bromosuccinimide (530 mg, 3.0 mmol). The reaction mixture is stirred at room temperature for 2 hrs. The reaction mixture is concentrated to give the crude product. Purification by flash column chromatography affords 680 mg of 6-bromo-5-chloro-1,2,3,4-tetrahydro-[1,8]naphthyridine.

후처리

  1. concentrationThe reaction mixture is concentrated
  2. customto give the crude product
  3. customPurification by flash column chromatography

출처 및 근거

ORD 기록
ord-518f038ee1934b28962cb8c8181f76ef
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181272B2

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