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HCID 86606218, 화합물 → [5-(3-Amino-phenyl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine

HRID 908177
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HRID 908177 반응식
[CH3:1][C:2]1[N:3]=[C:4]([NH:16][C:17]2[CH:22]=[N:21][CH:20]=[CH:19][N:18]=2)[S:5][C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-])=O)[CH:8]=1>C(OCC)(=O)C.C1COCC1.[Pd]>[NH2:13][C:9]1[CH:8]=[C:7]([C:6]2[S:5][C:4]([NH:16][C:17]3[CH:22]=[N:21][CH:20]=[CH:19][N:18]=3)=[N:3][C:2]=2[CH3:1])[CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86606218HCID 86606218, 화합물

생성물 1

HCID 85996839[5-(3-Amino-phenyl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine수율 36.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 21939870Tetrahydrofuran ethyl acetate용매

실험 절차

[4-Methyl-5-(3-nitro-phenyl)-thiazol-2-yl]-pyrazin-2-yl-amine (42b) (1.079 g, 3.4 mmol) is dissolved in ethyl acetate/THF (5/1, 240 ml) and stirred at room temperature under an atmosphere of argon. The solution is then treated with 10% Pd/C (1.1 g). The reaction mixture is purged three times with nitrogen and placed under an atmosphere of hydrogen overnight. The mixture is then filtered through celite and the catalyst is washed with THF (200 ml). The solvent is removed in vacuo to leave [5-(3-amino-phenyl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine (0.351 g, 36%). MH+ (ESMS):283.5

후처리

  1. customThe reaction mixture is purged three times with nitrogen
  2. filtrationThe mixture is then filtered through celite
  3. washthe catalyst is washed with THF (200 ml)
  4. customThe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-6a77bf69462244618ba2e7859c6a5f65
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017608B2

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