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Dimethyl Sulfoxide → HCID 53250722, 화합물

HRID 2170002
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HRID 2170002 반응식
Br[C:2]1[CH:7]=[N:6][CH:5]=[C:4]([Br:8])[N:3]=1.CS(C)=O.N12CCCN=C1CCCCC2.[OH:24][C:25]1[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=1[CH2:27][NH2:28]>C(OCC)(=O)C>[Br:8][C:4]1[N:3]=[C:2]([NH:28][CH2:27][C:26]2[CH:29]=[CH:30][CH:31]=[CH:32][C:25]=2[OH:24])[CH:7]=[N:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 702672-(Aminomethyl)phenol2회HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 203617002,6-Dibromopyrazine2회

생성물 1

HCID 53250722HCID 53250722, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Introduced into a 50 ml round-bottomed flask is 1 g (4.2 mmol) of 2,6-dibromopyrazine (starting material 3), to which 15 ml of dimethyl sulphoxide, 638 mg (4.2 mmol, 1eq) of 1,8-diazabicyclo[5.4.0]undec-7-ene, and 1.03 g (8.4 mmol, 2 eq) of 2-hydroxybenzylamine (starting material 4) are added; the mixture is left stirring for 2 h at room temperature. The reaction medium is diluted with 50 ml of ethyl acetate and then the mixture is washed with 50 ml of a saturated solution of ammonium chloride, and then twice with 50 ml of water. The organic phases are dried over magnesium sulphate, filtered and concentrated to dryness. The residue is purified by chromatography over silica with, as eluent, a heptane/ethyl acetate (8/2) mixture. 2-[(6-Bromopyrazin-2-ylamino)methyl]phenol is obtained in the form of a white solid.

후처리

  1. additionIntroduced into a 50 ml round-bottomed flask
  2. waitthe mixture is left
  3. washthe mixture is washed with 50 ml of a saturated solution of ammonium chloride
  4. dry with materialThe organic phases are dried over magnesium sulphate
  5. filtrationfiltered
  6. concentrationconcentrated to dryness
  7. customThe residue is purified by chromatography over silica with, as eluent

출처 및 근거

ORD 기록
ord-5135c05b7dde4f4bb1c52bbe13a6f158
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09050266B2

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