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Bromine → [2-(Bromoethyl)-6-(3-methoxyphenyl)pyrimidin-4-yl]-3-pyridylamine

HRID 30445
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반응식

HRID 30445 반응식
[CH2:1]([C:3]1[N:8]=[C:7]([NH:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:6]=[C:5]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=2)[N:4]=1)[CH3:2].C([O-])(=O)C.[Na+].[Br:29]Br>C(O)(=O)C>[Br:29][CH2:2][CH2:1][C:3]1[N:8]=[C:7]([NH:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:6]=[C:5]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=2)[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24408BromineHCID 517045Sodium AcetateHCID 59789711[2-Ethyl-6-(3-methoxyphenyl)pyrimidin-4-yl]-3-pyridylamine

생성물 1

HCID 86594232[2-(Bromoethyl)-6-(3-methoxyphenyl)pyrimidin-4-yl]-3-pyridylamine

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

[2-ethyl-6-(3-methoxyphenyl)pyrimidin-4-yl]-3-pyridylamine 14 (synthesized with a procedure similar to the one previously described) (1 eq) is dissolved in acetic acid, then sodium acetate (2 eq) is added. To this mixture, a solution of bromine (1 eq) in acetic acid is added dropwise. The reaction is stirred at room temperature for 3 h. The reaction mixture is concentrated under reduced pressure, water is added and the solution basified (pH ˜10-11) with sat. aq. Na2CO3 solution. The product 15 crashes out, is filtered off, dried, and used as is in the following step.

후처리

  1. concentrationThe reaction mixture is concentrated under reduced pressure, water
  2. additionis added
  3. filtrationThe product 15 crashes out, is filtered off
  4. customdried

출처 및 근거

ORD 기록
ord-8041afd55de144adb16b24e7672d0245
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07423148B2

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