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Methanol → 6-(Morpholin-4-yl)pyridine-3,4-diamine

HRID 1487999
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HRID 1487999 반응식
[N:1]1([C:7]2[CH:12]=[C:11]([NH2:13])[C:10]([N+:14]([O-])=O)=[CH:9][N:8]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.CO>[Pd].C1COCC1>[O:4]1[CH2:5][CH2:6][N:1]([C:7]2[N:8]=[CH:9][C:10]([NH2:14])=[C:11]([NH2:13])[CH:12]=2)[CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 887MethanolHCID 900216182-(Morpholin-4-yl)-5-nitropyridin-4-amine2회

생성물 1

HCID 900211616-(Morpholin-4-yl)pyridine-3,4-diamine수율 92.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

Into a 50-mL round-bottom flask were placed 2-(morpholin-4-yl)-5-nitropyridin-4-amine (compound 151.1, 350 mg, 1.56 mmol), methanol (20 mL), THF (10 mL), and Pd/C (35 mg). The above solution was purged with N2 and then H2. The reaction mixture was stirred for 4 h at room temperature. The solids were filtered out. The resulting mixture was concentrated under reduced pressure. This resulted in 280 mg (92%) of the title compound as a pink solid.

후처리

  1. customInto a 50-mL round-bottom flask were placed
  2. customThe above solution was purged with N2
  3. filtrationThe solids were filtered out
  4. concentrationThe resulting mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7e1d9f9f72884670bf1f31413599f3a7
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428502B2

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