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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175136Generated: October 29, 2026

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → Carbamic acid, N-[1-(6-hydroxy-3-quinolinyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/2175136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactanttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Bromoquinolin-6-yl acetateHCID 68530047—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
ProductCarbamic acid, N-[1-(6-hydroxy-3-quinolinyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl esterHCID 8669625612%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of Intermediate A (1.50 g, 5.07 mmol), tert-butyl pyrrolidin-3-ylcarbamate (1.13 g, 6.09 mmol), Pd2(dba)3 (0.232 g, 0.254 mmol), Xantphos (0.294 g, 0.507 mmol) and KOtBu (1.14 g, 10.2 mmol) in DMF (15 mL) was bubbled with argon for 20 min. The result mixture was heated at 110° C. overnight. The solution was cooled to rt and the solvent was removed under reduced pressure. The residue was diluted with water, extracted with DCM three times. The combined organic phase was dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography (eluting with 5% MeOH in DCM) to give the title compound as yellow solid (0.2 g, yield 11%). LCMS (method N): [M+H]+=330, tR=1.93 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062045B2
Source datasetuspto-grants-2015_06
ORD IDord-dc9dd3fcf64d4589bb1e0468547c6b64
Source noteuspto-grants-2015_06