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2-Amino-4,6-dimethyl pyrimidine → 2-Amino-5-bromo-4,6-dimethylpyrimidine

HRID 1846170
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인쇄 미리보기

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HRID 1846170 반응식
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[N:3]=1.[Br:10]N1C(=O)CCC1=O>C(#N)C>[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([Br:10])=[C:4]([CH3:9])[N:3]=1
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참가 물질

4

반응물 2

HCID 130212-Amino-4,6-dimethyl pyrimidineHCID 67184N-bromobutanimide

생성물 1

HCID 27377352-Amino-5-bromo-4,6-dimethylpyrimidine

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
23 °C

실험 절차

To a stirred solution containing 4.31 g (34.8 mmol) of 2-amino-4,6-dimethylpyrimidine in 150 mL of acetonitrile was added 6.15 g (52.1 mmol) of N-bromosuccinimide. The reaction mixture was stirred at 23° C. for 3 h. The formed precipitate was filtered and dried to afford the expected product as a colorless solid: yield 5.93 g (83%); mp 183-185° C.; silica gel TLC Rf 0.15 (2:1 ethyl acetate-hexanes); 1H NMR (CDCl3) δ 2.44 (s, 6H) and 5.19 (br s, 2H); 13C NMR (CDCl3) δ 24.7, 24.7, 109.6, 160.7, 160.7 and 166.3; mass spectrum (APCI), m/z 201.9982 (M+H)+ (C6H9N3Br requires 201.9980).

후처리

  1. filtrationThe formed precipitate was filtered
  2. customdried

출처 및 근거

ORD 기록
ord-10e3b24e2dae488fa62e6ab3c56a55d3
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952025B2

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