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Ethanamine, acetate → 2-ethylamino-5-isobutyl-6-methylpyrimid-4(3H)-one

HRID 1764425
노트
인쇄 미리보기

반응식

HRID 1764425 반응식
[CH2:1]([C:5]1[C:6](=[O:16])[NH:7][C:8]([NH:12][N+]([O-])=O)=[N:9][C:10]=1[CH3:11])[CH:2]([CH3:4])[CH3:3].[C:17](O)(=O)[CH3:18].C(N)C>O>[CH2:17]([NH:12][C:8]1[NH:7][C:6](=[O:16])[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[C:10]([CH3:11])[N:9]=1)[CH3:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12203875Ethanamine, acetateHCID 1363884225-isobutyl-6-methyl-2-nitraminopyrimid-4(3H)-one

생성물 1

HCID 1357355932-ethylamino-5-isobutyl-6-methylpyrimid-4(3H)-one

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
120 °C

실험 절차

5-Isobutyl-6-methyl-2-nitraminopyrimid-4(3H)-one (16.0 g) was mixed with ethylamine acetate (30 g) and heated without solvent at 120° C for 6 hours. The melt was cooled and water was added. The mixture was brought to pH 5 and the precipitated product recrystallised from aqueous acetone to give 2-ethylamino-5-isobutyl-6-methylpyrimid-4(3H)-one (formula VII, R1 = CH3, R = is C4H9, R6 = H, R7 = C2H5) having a melting point of 203°-204° C.

후처리

  1. temperatureThe melt was cooled
  2. customthe precipitated product recrystallised from aqueous acetone

출처 및 근거

ORD 기록
ord-9efda7967c1f4c6289b5252603162d76
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04116674

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