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Methanol → HCID 505743, 화합물

HRID 1883547
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HRID 1883547 반응식
CO.C(O[C:6]([C:8]1[C:9]([NH:16][C:17]2[CH:18]=[C:19]3[C:23](=[CH:24][CH:25]=2)[NH:22][N:21]=[CH:20]3)=[N:10][C:11]([S:14][CH3:15])=[N:12][CH:13]=1)=[O:7])C.[CH2:26]([NH2:28])[CH3:27]>O>[CH2:26]([NH:28][C:6]([C:8]1[C:9]([NH:16][C:17]2[CH:18]=[C:19]3[C:23](=[CH:24][CH:25]=2)[NH:22][N:21]=[CH:20]3)=[N:10][C:11]([S:14][CH3:15])=[N:12][CH:13]=1)=[O:7])[CH3:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 6341EthylamineHCID 11209679HCID 11209679, 화합물

생성물 1

HCID 505743HCID 505743, 화합물수율 80%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To the solution of methanol (20 ml) was added 4-(1H-5-indazolylamino)-2-methylthio-5-pyrimidinecarboxylic acid ethyl ester (1 g) prepared from preparation example 1, added70% aq. ethylamine (25ml) at room temperatute, and reacted at 30-35° C. for 3 hr. The reaction mixture was cooled and slowly added H2O (30 ml) and stirred for 0.5 hr. The reaction mixture was filtered, washed with 30% aqueous methanol solution (10 ml) obtained the desired compound (0.8 g, 80%)

후처리

  1. customreacted at 30-35° C. for 3 hr
  2. temperatureThe reaction mixture was cooled
  3. filtrationThe reaction mixture was filtered
  4. washwashed with 30% aqueous methanol solution (10 ml)

출처 및 근거

ORD 기록
ord-d6c6b699dd7a4cbf9c9de403ffff37d5
출처 데이터셋
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06762189B1

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