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2,4-Diamino-5-(1-benzyl-4-piperidinyl)pyrimidine → HCID 22461017, 화합물

HRID 623198
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HRID 623198 반응식
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH:9]2[CH2:14][CH2:13][N:12](CC3C=CC=CC=3)[CH2:11][CH2:10]2)=[CH:4][N:3]=1>C(O)C.C(O)(=O)C.[Pd]>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 224610192,4-Diamino-5-(1-benzyl-4-piperidinyl)pyrimidine

생성물 1

HCID 22461017HCID 22461017, 화합물

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 176Acetic Acid용매HCID 702Ethanol용매

실험 절차

A solution of 26 g of 2,4-diamino-5-(1-benzyl-4-piperidinyl)pyrimidine in 700 ml of ethanol and 20 ml of acetic acid was hydrogenated over 5 g of Pd/C 10% at room temperature and normal pressure up to the standstill of the hydrogen uptake, whereupon it was filtered off from catalyst. The filtrate was concentrated and the crystalline residue was dissolved in 100 ml of water. Chromatography on Dowex 1 (×10 200-400 mesh) (a cation exchange resin) gave 2,4-diamino-5-(4-piperidyl)-pyrimidine of melting point 230°-231° C. (dec.) (from water).

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후처리

  1. filtrationnormal pressure up to the standstill of the hydrogen uptake, whereupon it was filtered off from catalyst
  2. concentrationThe filtrate was concentrated
  3. dissolutionthe crystalline residue was dissolved in 100 ml of water

출처 및 근거

ORD 기록
ord-1892080e9cfb47348e714197794aeae6
출처 데이터셋
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04774249

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