反应详情
EQUATION
反应方程式
REACTANTS
反应物
Triphenylphosphine oxide
C18H15OP
Trifluoromethanesulfonic anhydride
C2F6O5S2
1-Hydroxybenzotriazole
C6H5N3O
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
2-[(Triphenylmethyl)sulfanyl]ethan-1-amine--hydrogen chloride (1/1)
C21H22ClNS
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a mixture of 4-ethyl-6-[methyl(2-thienylsulfonyl)amino]-1,4-dihydropyrrolo[3,2-b]pyrrole-2-carboxylic acid (780 mg), 2-(tritylthio)ethaneamine hydrochloride (850 mg), 1H-1,2,3-benzotriazol-1-ol (370 mg), triethylamine (0.5 mL) and N,N-dimethylformamide (15 mL) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (460 mg), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated to give a colorless oil. To a solution of triphenylphosphine oxide (1.8 g) in dichloromethane (20 mL) was slowly added trifluoromethanesulfonic anhydride (555 μL) at 0° C., the mixture was stirred for 10 min, and the colorless oil was added. The reaction mixture was stirred at room temperature for 2 hr and concentrated. Saturated aqueous sodium hydrogen carbonate was added thereto, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to give N-[5-(4,5-dihydro-1,3-thiazol-2-yl)-1-ethyl-1,4-dihydropyrrolo[3,2-b]pyrrol-3-yl]-N-methylthiophene-2-sulfonamide (260 mg, yield 30%) as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:20 to 1:3, volume ratio). melting point 163° C.
WORKUP
后处理
- extractionthe mixture was extracted with ethyl acetate
- washThe ethyl acetate layer was washed with saturated brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customto give a colorless oil
- customat 0° C.
- stirringthe mixture was stirred for 10 min
- additionthe colorless oil was added
- stirringThe reaction mixture was stirred at room temperature for 2 hr
- concentrationconcentrated
- additionSaturated aqueous sodium hydrogen carbonate was added
- extractionthe mixture was extracted with ethyl acetate
- washThe ethyl acetate layer was washed with saturated brine
- dry with materialdried (MgSO4)
- concentrationconcentrated