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4-Chlorobenzaldehyde → 6-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dione

HRID 2200541
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HRID 2200541 반응식
[NH2:1][C:2]1[C:3](=[O:11])[N:4]([CH3:10])[C:5](=[O:9])[NH:6][C:7]=1[NH2:8].[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH:17]=O)=[CH:15][CH:14]=1.C([BH3-])#N.[Na+]>O.C(O)(=O)C>[NH2:8][C:7]1[NH:6][C:5](=[O:9])[N:4]([CH3:10])[C:3](=[O:11])[C:2]=1[NH:1][CH2:17][C:16]1[CH:19]=[CH:20][C:13]([Cl:12])=[CH:14][CH:15]=1
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참가 물질

6

반응물 3

HCID 77264-ChlorobenzaldehydeHCID 1201412SS-3364HCID 5003444Sodium cyanoborohydride

생성물 1

HCID 904032716-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dione수율 42.9%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water
용매

실험 절차

To a solution of 5,6-diamino-3-methylpyrimidine-2,4(1H,3H)-dione (0.8 g, 5.13 mmol) in water (10 mL) and acetic acid (0.5 mL) was added 4-chlorobenzaldehyde (0.72 g, 5.14 mmol), the mixture was stirred at room temperature for 5 h. The mixture was cooled to 0° C., sodium cyanoborohydride (0.3 g, 4.76 mmol) was added and the resulting mixture was stirred at room temperature overnight. The mixture was concentrated and filtered, and the filter cake was washed with methanol, dried in vacuo to give 6-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dione (0.6 g, 42.9% yield) as yellow solid. LCMS MH+ 281.

후처리

  1. temperatureThe mixture was cooled to 0° C.
  2. stirringthe resulting mixture was stirred at room temperature overnight
  3. concentrationThe mixture was concentrated
  4. filtrationfiltered
  5. washthe filter cake was washed with methanol
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-326c75503d254cf799e33f299497d0a6
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09359359B2

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