HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Amino-1H-pyrrol-2-yl)-(3-methyl-2-thienyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-[(3-Methyl-2-thienyl)carbonyl-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dion | HCID 19973160 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1-Amino-1H-pyrrol-2-yl)-(3-methyl-2-thienyl)methanone | HCID 19973163 | 79.4% |
Reaction Steps
To a solution consisting of 2-[2-[(3-methyl-2-thienyl)carbonyl]-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dione (11.5 g) in DMF (30 ml) was added 40% methylamine (aq., 34.0 ml) solution at room temperature. The reaction mixture was stirred at ambient temperature for 3.5 hours, then poured into water and ethyl acetate. The layers were separated and the aqueous phase was extracted thrice with EtOAc. The combined organics were washed with water, brine, and dried (MgSO4). Filtration and concentration gave the crude product. Purification via preparative HPLC (silica gel, 2:1 heptane/EtOAc), followed by crystallization from ether/pentane afforded 5.6 g of the product as a solid, m.p. 42°-44° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05274116 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-d0a5a95303c1443ba7ca6f8a72dd4f4a |
| Source note | uspto-grants-1993_12 |