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Hydrochloric Acid → (4-Methoxy-6-methylpyrimidin-2-YL)methanamine

HRID 2413080
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HRID 2413080 반응식
[C:1]([C:3]1[N:8]=[C:7]([CH3:9])[CH:6]=[C:5]([O:10][CH3:11])[N:4]=1)#[N:2].Cl>[Pd].CO>[NH2:2][CH2:1][C:3]1[N:8]=[C:7]([CH3:9])[CH:6]=[C:5]([O:10][CH3:11])[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 123850914-Methoxy-6-methylpyrimidine-2-carbonitrile

생성물 1

HCID 13392683(4-Methoxy-6-methylpyrimidin-2-YL)methanamine수율 39.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of 4.4 g of the product from Example 8, 0.35 g 10% palladium-on-carbon catalyst, and 1.5 ml of concentrated hydrochloric acid in 70 ml methanol was shaken under an atmosphere of hydrogen at 46 p.s.i. on a Parr Hydrogenation Apparatus. After 31/2 hours, the solution was filtered through a pad of Celite and the filtrate was concentrated in vacuo. The resulting solid was taken up in water and the aqueous layer was washed with several small portions of ether. Adjustment to pH 13 followed by extraction with methylene chloride, drying, and evaporation of the organic layer gave 1.8 g of the title compound as a light yellowish-orange oil.

후처리

  1. filtrationAfter 31/2 hours, the solution was filtered through a pad of Celite
  2. concentrationthe filtrate was concentrated in vacuo
  3. washthe aqueous layer was washed with several small portions of ether
  4. extractionfollowed by extraction with methylene chloride
  5. customdrying
  6. customevaporation of the organic layer

출처 및 근거

ORD 기록
ord-205768a1d9714eb6a3ba38830ef17349
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04496392

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