HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911465Generated: October 27, 2026
Hexahydro-1,4-diazepine → Ethyl 5-(4-ethylpiperazin-1-yl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1911465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | Ethyl 5-bromothiophene-2-carboxylate | HCID 605723 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 5-(4-ethylpiperazin-1-yl)thiophene-2-carboxylate | HCID 66589785 | 17% |
Reaction Steps
Palladium(II) acetate (52.1 mg, 0.23 mmol) followed by sodium tert-butoxide (624 mg, 6.49 mmol) was added to a stirred solution of ethyl 5-bromothiophene-2-carboxylate (1090 mg, 4.64 mmol), homopiperazine (511 mg, 5.10 mmol) and (rac)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (289 mg, 0.46 mmol) in toluene (20 mL) at 25° C. under nitrogen. The resulting suspension was stirred at 110° C. for 3 h. The cooled reaction mixture was diluted with MeOH and the crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions containing the desired product were evaporated to dryness to afford impure product as a brown oil. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 7N NH3/MeOH in DCM and then 0 to 3% NH3/MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(4-ethylpiperazin-1-yl)thiophene-2-carboxylate (195 mg, 17%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08604022B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-dcb93875f93d4b218576d288c06047ac |
|---|
| Source note | uspto-grants-2013_12 |
|---|