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. 2022 Nov 28;18:1607–1616. doi: 10.3762/bjoc.18.171

Table 2.

One-pot reaction for the synthesis of compound 7.

graphic file with name Beilstein_J_Org_Chem-18-1607-i002.jpg

entry Ar1 Ar2 R1 product yield (%)b

1 2-thiophenyl 3-OMe-4-FC6H3 CO2Et 7a 66
2 2-thiophenyl 2-furanyl CO2Et 7b 51
3 2-thiophenyl 3-pyridinyl CO2Et 7c 43
4 2-FC6H4 4-ClC6H4 CO2Et 7d 72
5 4-BrC6H4 4-ClC6H4 CO2Et 7e 66
6 4-BrC6H4 Ph COMe 7f trace
7 4-BrC6H4 Ph Ph 7g
8 4-BrC6H4 CO2Et CO2Et 7h messy
9 4-BrC6H4 ethyl CO2Et 7i messy

aIsolated yield. Reaction conditions are same as Table 1, entry 5.