HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 3-methoxyphenyl ketone → 2-Amino-3-ethoxycarbonyl-5-(3-methoxy-phenyl)-1H-pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 3-methoxyphenyl ketone | HCID 101294 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-carbamimidoylacetate hydrochloride | HCID 15555354 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-3-ethoxycarbonyl-5-(3-methoxy-phenyl)-1H-pyrrole | HCID 23282732 | — |
Reaction Steps
Analogously to Step 8.1, 14.5 g (87 mmol) of 2-amidino-acetic acid ethyl ester hydro-chloride in 150 ml of abs. ethanol are reacted with 5.9 g (87 mmol) of sodium ethanolate and 10.3 g (44 mmol) of 2-bromo-1-(3-methoxy-phenyl)-ethan-1-one (2-bromo-3'-methoxy-acetophenone; Janssen) to form the title compound; m.p. 96-97oC; TLC-Rf =0.2 (hexane/ethyl acetate [2:1]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140332 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-1e6174638c374ddca4eafe2c8c0c7541 |
| Source note | uspto-grants-2000_10 |