反应详情

0.116 g of (2-{(E)-3-[1-(toluene-4-sulfonyl)-1-H-pyrrol-3-yl]-allanoylamino}-phenyl)-carbamic acid tert-butyl ester (compound A5) are dissolved in 20 ml of dichloromethane at ambient temperature. 2 ml of trifluoroacetic acid (TFA) are added and the solution is stirred for 93 hour. The solvent is evaporated to dryness and to the residue are added 25 ml of water. The water phase is extracted exhaustively with ethyl acetate. Afterwards the combined organic phases are dried over sodium sulfate and filtered. The filtrate is evaporated under vacuo. Then the residue is crystallized from methanol to give 0.050 g of the title compound as white crystals.

1. customThe solvent is evaporated to dryness and to the residue
2. additionare added 25 ml of water
3. extractionThe water phase is extracted exhaustively with ethyl acetate
4. dry with materialAfterwards the combined organic phases are dried over sodium sulfate
5. filtrationfiltered
6. customThe filtrate is evaporated under vacuo
7. customThen the residue is crystallized from methanol