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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-t-butylphosphine fluoroborateHCID 44558591—
ReactantBenzyl 2,4-bis(benzyloxy)-6-chloro-5-ethylnicotinateHCID 86280413—
Reactanttert-butyl (7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-2-yl)carbamateHCID 123500811—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventDimethyl SulfoxideHCID 679—
Productbenzyl 2,4-bis(benzyloxy)-6-(2-((tert-butoxycarbonyl)amino)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-7-yl)-5-methylnicotinateHCID 7128434255.1%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-11ac0a5b038c4268836630ce05dbdad4
Source noteuspto-grants-2016_08