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Ethanolamine → HCID 505745, 화합물

HRID 1883549
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반응식

HRID 1883549 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]([CH2:28][NH2:29])[OH:27]>O>[OH:27][CH2:26][CH2:28][NH:29][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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 887MethanolHCID 11209679HCID 11209679, 화합물

생성물 1

HCID 505745HCID 505745, 화합물수율 72%

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, added ethanol amine (7 ml) at room temperature, and refluxed for 4 hr. The reaction mixture was cooled and slowly added H2O (40 ml) at 20° C. and stirred for 0.5 hr. The reaction mixture was filtered, washed with 25% aqueous methanol solution (10 ml), obtained the desired compound (0.75 g, 72%)

후처리

  1. customprepared from preparation example 1
  2. temperaturerefluxed for 4 hr
  3. temperatureThe reaction mixture was cooled
  4. filtrationThe reaction mixture was filtered
  5. washwashed with 25% aqueous methanol solution (10 ml)

출처 및 근거

ORD 기록
ord-5b981ed768b8491a9a20bc91c7ba82ce
출처 데이터셋
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06762189B1

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