HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092115Generated: October 31, 2026
Cesium carbonate → Ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1092115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | Ethyl 5-bromothiophene-2-carboxylate | HCID 605723 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylate | HCID 66589793 | 12.7% |
Reaction Steps
Palladium(II)acetate (0.135 g, 0.60 mmol) was added to ethyl 5-bromothiophene-2-carboxylate (1.411 g, 6 mmol), 1-methyl-1,4-diazepane (0.822 g, 7.20 mmol), BINAP (0.374 g, 0.60 mmol) and cesium carbonate (2.74 g, 8.40 mmol) in dioxane (40 mL) warmed to 80° C. for 18 h under nitrogen. The crude reaction mixture was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH. Fractions were evaporated to dryness to afford the crude product. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 3M ammonia/MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylate (0.204 g, 12.67%) as a yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129391B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-cce7dcfe6cfc49e280e1449cb0b0dea7 |
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| Source note | uspto-grants-2012_03 |
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