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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870376Generated: November 2, 2026

Binap, (A+-)- → HCID 68915125, compound

https://huagongshe.com/reaction/870376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant3-FluoropyrrolidineHCID 2759163—
ReactantHCID 68916958HCID 68916958—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68915125HCID 6891512547%

Reaction Steps

Buchwald coupling reaction using (R)-3-fluoropyrrolidine, Reaction of 0.200 g of [(S)-6-(4-bromo-benzenesulfonylamino)-1,2,3,4-tetrahydronaphthalen-2-yl]-propyl-carbamic acid tert-butyl ester (0.38 mmol), 72 mg of (R)-3-fluoropyrrolidine (0.57 mmol), 51 mg of NaOtC4H9 (1.53 mmol), 39 mg of Pd2(dba)3 (tris(dibenzylideneacetone)dipalladium(0) (0.04 mmol)), 47 mg of BINAP (2,2′-bis(diphenylphosphino)-1,1′-binaphthyl) (0.08 mmol) in 5 ml tetrahydrofuran at 80° C. for 48 hours yielded 95 mg (47%) of {(S)-6-[4-((R)-3-fluoro-pyrrolidin-1-yl)benzenesulfonylamino]-1,2,3,4-tetrahydro-naphthalen-2-yl}-propyl-carbamic acid tert-butyl ester as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969552B2
Source datasetuspto-grants-2015_03
ORD IDord-1708ab016e1245679f41c539321b2958
Source noteuspto-grants-2015_03