Formic Acid → 2-(2,6-Dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine

HRID 474297ノート

反応式

HRID 474297 の反応式
Cl[C:2]1[C:7]([NH:8][C:9](=O)[CH2:10][C:11]2[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:18])=[C:6](Cl)[N:5]=[C:4]([S:21][CH3:22])[N:3]=1.NC(N)=[S:25].[CH3:27][CH2:28][OH:29].[CH:30]([OH:32])=O>>[Cl:18][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([Cl:17])[C:11]=1[CH2:10][C:9]1[S:25][C:2]2[N:3]=[C:4]([S:21][CH3:22])[N:5]=[C:30]([OH:32])[C:7]=2[N:8]=1.[Cl:18][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([Cl:17])[C:11]=1[CH2:10][C:9]1[S:25][C:2]2[N:3]=[C:4]([S:21][CH3:22])[N:5]=[C:6]([O:29][CH2:28][CH3:27])[C:7]=2[N:8]=1

参加物

6

反応条件

温度
90 °C

実験手順

To a mixture of N-(4,6-dichloro-2-methylsulfanyl-pyrimidin-5-yl)-2-(2,6-dichloro-phenyl)-acetamide (10 g, 25 mmol), thiourea (1.9 g, 25 mmol), and EtOH (100 mL) was added formic acid (0.8 mL) at rt. The resulting mixture was heated to 90° C. After 12 h, the reaction mixture was cooled and concentrated. The resulting residue was collected by vacuum filtration and washed with H2O (50 mL) followed by hexanes (50 mL). The title compound purified by FCC to afford 2-(2,6-dichloro-benzyl)-5-methylsulfanyl-thiazolo[5,4-d]pyrimidin-7-ol (1.6 g, 18%) and 2-(2,6-dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine (4 g, 41%) as colorless solids.

後処理

  1. temperaturethe reaction mixture was cooled
  2. concentrationconcentrated
  3. filtrationThe resulting residue was collected by vacuum filtration
  4. washwashed with H2O (50 mL)
  5. customThe title compound purified by FCC

出典と根拠

ORDレコード
ord-2ee5316fe2d1484d84b037226153518d
出典データセット
uspto-grants-2014_01
特許番号
US08637527B2

反応ノート

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