HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58193Generated: October 26, 2026
Cesium carbonate → Tert-butyl (4-(4-isopropylpiperazin-1-yl)-2-nitrophenyl)carbamate
https://huagongshe.com/reaction/58193
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | tert-Butyl (4-bromo-2-nitrophenyl)carbamate | HCID 52904808 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl (4-(4-isopropylpiperazin-1-yl)-2-nitrophenyl)carbamate | HCID 118034135 | 70.5% |
Reaction Steps
1-isopropylpiperazine (1.29 g, 5.66 mmol) and tert-butyl (4-bromo-2-nitrophenyl)carbamate (1.5 g, 4.71 mmol) were taken in a mixture of dry toluene (15 mL) and dioxane (2 mL) in a seal tube under argon atmosphere at room temperature. The Argon gas was purged for 5-10 min. Then Cs2CO3 (3.06 g, 9.43 mmol) and Xantphos (0.54 g, 0.94 mmol) were added and the resulting reaction mixture was purged with argon gas for 5 min., followed by Pd2(dba)3 (0.43 g, 0.47 mmol). The argon gas purging was continued for additional 5 min. before sealing the reaction vial. Then the reaction mixture was heated at 100° C. for 12 hr. After completion of the reaction by TLC, the reaction mixture was cooled to room temperature, filtered through celite bed and concentrated. The residue was purified by silica gel column chromatography (DCM:MeOH/97:3) to afford the title compound (1.2 g, yield: 70.5%). MS (ESI): 365.5 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434697B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-d42be63aa535499088173e15186d4576 |
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| Source note | uspto-grants-2016_09 |
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