HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481792Generated: November 1, 2026
Potassium Carbonate → benzyl 2,4-bis(benzyloxy)-6-(2-((tert-butoxycarbonyl)amino)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-7-yl)-5-methylnicotinate
https://huagongshe.com/reaction/1481792
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tri-t-butylphosphine fluoroborate | HCID 44558591 | — |
| Reactant | Benzyl 2,4-bis(benzyloxy)-6-chloro-5-ethylnicotinate | HCID 86280413 | — |
| Reactant | tert-butyl (7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-2-yl)carbamate | HCID 123500811 | — |
| Catalyst | Tris(dibenzylideneacetone) dipalladium | HCID 9832798 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | benzyl 2,4-bis(benzyloxy)-6-(2-((tert-butoxycarbonyl)amino)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-7-yl)-5-methylnicotinate | HCID 71284342 | 55.1% |
Reaction Steps
The intermediate from Step 2 (280 mg, 0.7 mmol) was combined with benzyl 2,4-bis(benzyloxy)-6-chloro-5-methylnicotinate (332 mg, 0.7 mmol, prepared according to Example 379, Step 3), potassium carbonate (193 mg, 1.4 mmol), tris(dibenzylideneacetone) dipalladium(0) (32 mg, 0.035 mmol) and tri-tert-butylphosphine tetrafluoroborate (41 mg, 0.14 mmol) in DMSO (3 mL). The mixture was heated under Ar at 120° C. for 20 min. The mixture was cooled to room temperature and partitioned in CH2Cl2 (10 mL) and saturated aqueous NaHCO3 (10 mL). The organic layer was removed, concentrated and chromatographed on silica gel (0-30% EtOAc in hexanes) to provide the product as a white powder (274 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409905B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-11ac0a5b038c4268836630ce05dbdad4 |
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| Source note | uspto-grants-2016_08 |
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