2-Aminothiazole → 6-(5-(phenylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine

HRID 1366234

反応式

HRID 1366234 の反応式
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[C:7]1([C:13]#[C:14][C:15]2[S:19][C:18]([CH:20]=O)=[CH:17][CH:16]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:22][C:23]([N+:30]#[C-:31])([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])[CH3:24].Cl(O)(=O)(=O)=O.C([O-])([O-])=O.[Na+].[Na+]>C(Cl)Cl>[C:7]1([C:13]#[C:14][C:15]2[S:19][C:18]([C:20]3[N:1]=[C:2]4[N:6]([C:31]=3[NH:30][C:23]([CH3:24])([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])[CH3:22])[CH:5]=[CH:4][S:3]4)=[CH:17][CH:16]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

参加物

7

実験手順

A solution of 400 mg (4.0 mmol) 2-aminothiazole, 1018 mg (4.8 mmol) 5-phenylethynyl-thiophene-2-carbaldehyde, 557 mg (4.0 mmol) (2,4,4-trimethylpentane-2-yl)-isocyanide and 400 μl of a 20% aq. perchloric acid was stirred in DCM (8 ml) for 5 d at RT. A 1 molar aq. Na2CO3 sol. was subsequently added. The phases were separated and the aqueous phase was extracted with DCM. The collected organic phases were washed with brine and dried over MgSO4. After filtering and removal of the solvent in a vacuum, a CC (AE/hexane 1:4) was performed with the residue, whereby 637 mg (1.47 mmol, 37%) 6-(5-(phenylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine was obtained.

後処理

  1. customThe phases were separated
  2. extractionthe aqueous phase was extracted with DCM
  3. washThe collected organic phases were washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationAfter filtering
  6. customremoval of the solvent in a vacuum

出典と根拠

ORDレコード
ord-a2845a41776046949978bb693ed40b77
出典データセット
uspto-grants-2011_02
特許番号
US07893069B2

関連ノート

読み込み中…