HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-(2-Chlorophenyl)-2-ethyl-5-nitrothieno[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-(2-Chlorobenzoyl)-2-(2-nitroethenylamino)-5-ethylthiophene | HCID 67757398 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Benzene dioxane | HCID 69021906 | — |
| Product | 4-(2-Chlorophenyl)-2-ethyl-5-nitrothieno[2,3-b]pyridine | HCID 19787168 | 89.1% |
Reaction Steps
To a solution of DBU (5.1 g) in benzene (50 ml) was added dropwise a solution of 3-(2-chlorobenzoyl)-2-(2-nitroethenylamino)-5-ethylthiophene (5.1 g) in dioxane-benzene (1 : 1, 30 ml}over one hour with stirring under reflux. After refluxing for additional one hour, the mixture was washed with water and dried over MgSO4. The solvent was distilled off and to the residue was added isopropyl ether to obtain 4-(2-chlorophenyl)-2-ethyl-5-nitrothieno[2,3-b]pyridine as crystals (4.3 g, 89.0%). The crystals were recrystallized from isopropyl ether to obtain pale yellow prisms, mp: 72°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05143919 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-878f80ccbce24f218606802f277ae8e6 |
| Source note | uspto-grants-1992_09 |