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Hydrochloride methanol → 1,4,5,6-Tetrahydro-N-methoxy-5-pyrimidinamine dihydrochloride

HRID 129821
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HRID 129821 반응식
[ClH:1].[CH3:2][O:3][N:4]=[C:5]1[CH2:10][NH:9][CH:8]=[N:7][CH2:6]1.Cl.CO.[BH4-].CN(C)C>CO>[ClH:1].[ClH:1].[CH3:2][O:3][NH:4][CH:5]1[CH2:10][NH:9][CH:8]=[N:7][CH2:6]1
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참가 물질

5

반응물 3

HCID 21893726Hydrochloride methanolHCID 736056051,6-Dihydro-5(4H)-pyrimidinone O-methyloxime monohydrochlorideHCID 131719211Trimethylamine borohydride

생성물 1

HCID 193704701,4,5,6-Tetrahydro-N-methoxy-5-pyrimidinamine dihydrochloride수율 38%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 1,6-dihydro-5-(4H)-pyrimidinone O-methyloxim monohydrochloride (2.8 g, 17.1 mmol) in dry methanol was added dropwise to a stirred solution of HCl/methanol (49 ml of a 3N solution) and trimethylamine borohydride (1.36 g, 18.7 mmol) at room temperature under a nitrogen atmosphere. After 1 hour the reaction product crystallised spontaneously. Recrystallization from methanol/ethyl acetate gave a light-brown material in 38% yield (1.30 g). Mp. 214.0° C.

후처리

  1. customAfter 1 hour the reaction product crystallised spontaneously
  2. customRecrystallization from methanol/ethyl acetate
  3. customgave a light-brown material in 38% yield (1.30 g)

출처 및 근거

ORD 기록
ord-5d150106284f449cb8c5312a003774d5
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05470856

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