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Pyridine → HCID 44539724, 화합물

HRID 1695800
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HRID 1695800 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([C:11]2[CH:12]=[C:13]([NH:18][S:19]([CH3:22])(=[O:21])=[O:20])[C:14]([Cl:17])=[N:15][CH:16]=2)[CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][N:6]2[CH3:23].N1C=CC=CC=1.[CH3:30][C:31]1[S:32][CH:33]=[C:34]([C:36](Cl)=[O:37])[N:35]=1.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[Cl:17][C:14]1[N:15]=[CH:16][C:11]([C:9]2[CH:8]=[C:7]3[C:3]([CH:4]=[N:5][N:6]3[CH3:23])=[C:2]([NH:1][C:36]([C:34]3[N:35]=[C:31]([CH3:30])[S:32][CH:33]=3)=[O:37])[CH:10]=2)=[CH:12][C:13]=1[NH:18][S:19]([CH3:22])(=[O:21])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 516892Sodium BicarbonateHCID 211839592-Methyl-1,3-thiazole-4-carbonyl chlorideHCID 86653304HCID 86653304, 화합물

생성물 1

HCID 44539724HCID 44539724, 화합물수율 1.5%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매
3회

실험 절차

N-[5-(4-Amino-1-methyl-1H-indazol-6-yl)-2-chloro-3-pyridinyl]methanesulfonamide (75 mg) was dissolved in DCM (2 ml) and pyridine (0.052 ml) was added followed by 2-methyl-1,3-thiazole-4-carbonyl chloride (52 mg) in DCM (1 ml) as a suspension. The reaction was stirred at RT for 1 h. Saturated sodium bicarbonate solution was added followed by DCM (3 ml) and the reaction was stirred vigorously. The reaction was passed through a hydrophobic frit and evaporated to dryness. The residue was dissolved in DMSO:MeOH (1:1, v/v, 1 ml) and purified by MDAP (method E) to give the title compound (1.5 mg).

후처리

  1. stirringthe reaction was stirred vigorously
  2. customevaporated to dryness
  3. dissolutionThe residue was dissolved in DMSO:MeOH (1:1, v/v, 1 ml)
  4. custompurified by MDAP (method E)

출처 및 근거

ORD 기록
ord-44ad09fa1b1142dbb9f3187d03e2f4b8
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163743B2

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