반응식
[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]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
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.
후처리
- customThe phases were separated
- extractionthe aqueous phase was extracted with DCM
- washThe collected organic phases were washed with brine
- dry with materialdried over MgSO4
- filtrationAfter filtering
- customremoval of the solvent in a vacuum
출처 및 근거
- ORD 기록
- ord-a2845a41776046949978bb693ed40b77
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07893069B2
연결된 노트
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