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3-Methoxypropylamine → 4,6-Dichloro-N-(3-methoxypropyl)pyrimidin-2-amine

HRID 1248885
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HRID 1248885 반응식
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][NH2:6].Cl[C:8]1[N:13]=[C:12]([Cl:14])[CH:11]=[C:10]([Cl:15])[N:9]=1>O1CCCC1>[Cl:15][C:10]1[CH:11]=[C:12]([Cl:14])[N:13]=[C:8]([NH:6][CH2:5][CH2:4][CH2:3][O:2][CH3:1])[N:9]=1
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참가 물질

4

반응물 2

HCID 16723-MethoxypropylamineHCID 773782,4,6-Trichloropyrimidine

생성물 1

HCID 136496914,6-Dichloro-N-(3-methoxypropyl)pyrimidin-2-amine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

48 g (0.54 mole) of 3-methoxypropylamine are added dropwise to 50 g (0.27 mole) of 2,4,6-trichloropyrimidine, dissolved in 300 ml of tetrahydrofuran, at -30° C. After the reaction mixture has thawed to room temperature and been stirred for a further six hours, it is poured into ice water and extracted with methylene chloride, the extract is dried over sodium sulphate and the solvent is removed. The resulting residue is subjected to steam distillation in the course of which 10.6 g (16.6% of theory) of the desired pyrimidine pass over as a solid, melting point 48° C.

후처리

  1. customhas thawed to room temperature
  2. extractionextracted with methylene chloride
  3. dry with materialthe extract is dried over sodium sulphate
  4. customthe solvent is removed
  5. distillationThe resulting residue is subjected to steam distillation in the course of which 10.6 g (16.6% of theory) of the desired pyrimidine pass over as a solid, melting point 48° C.

출처 및 근거

ORD 기록
ord-2f1d646afc524ab9942ddc9a13be653d
출처 데이터셋
uspto-grants-1986_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04627872

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