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3-Amino-1,2-propanediol → HCID 15860289, 화합물

HRID 2184773
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HRID 2184773 반응식
CO[C:3]([C:5]1[CH:10]=[N:9][C:8]([C:11]([O:13]C)=O)=[CH:7][N:6]=1)=[O:4].[NH2:15][CH2:16][CH:17]([OH:20])[CH2:18][OH:19]>C(O)C>[OH:20][CH:17]([CH2:18][OH:19])[CH2:16][NH:15][C:11]([C:8]1[CH:7]=[N:6][C:5]([C:3]([NH:15][CH2:16][CH:17]([OH:20])[CH2:18][OH:19])=[O:4])=[CH:10][N:9]=1)=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 735613-Amino-1,2-propanediolHCID 518685Dimethyl pyrazine-2,5-dicarboxylate

생성물 1

HCID 15860289HCID 15860289, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 490 mg of 2,5-dimethoxycarbonylpyrazine and 0.40 cm3 of 3-amino-1,2-propanediol in 5 cm3 of ethanol is heated at a temperature in the region of the reflux temperature for 3 hours. The reaction mixture is filtered while hot. The white solid is washed with 3 times 15 cm3 of boiling ethanol. 416 mg of N,N′-bis(2,3-dihydroxy-1-propyl)pyrazine-2,5-dicarboxamide are thus obtained in the form of a white solid melting at 234° C. [1H NMR spectrum (400 MHz, (CD3)2SO-d6, δ in ppm): from 3.20 to 3.60 (mt, 8H: 2×OCH2 and 2×NCH2); 3.68 (mt, 2H: 2×OCH); 4.67 (t, J=5.5 Hz, 2H: OH at 2γ and OH at 5γ); 4.95 (d, J=5 Hz, 2H: OH at 2β and OH at 5β); 8.79 (t, J=5.5 Hz, 2H: 2×CONH); 9.23 (s, 2H: ═CH at 3 and ═CH at 6)].

후처리

  1. filtrationThe reaction mixture is filtered while hot
  2. washThe white solid is washed with 3 times 15 cm3 of boiling ethanol

출처 및 근거

ORD 기록
ord-dc06b648f69448f08610f30a455ae60d
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399613B1

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