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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335929Generated: October 26, 2026

Lithium Hexamethyldisilazide → (S)-3-(3,3-difluoropyrrolidin-1-yl)-7-(pyridin-3-yl)-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amine

https://huagongshe.com/reaction/335929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant3,3-Difluoropyrrolidine hydrochlorideHCID 24903482—
Reactant(S)-3-chloro-7-(pyridin-3-yl)-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amineHCID 58466185—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-(3,3-difluoropyrrolidin-1-yl)-7-(pyridin-3-yl)-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amineHCID 58466327—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a resealable tube charged with a mixture of (S)-3-chloro-7-(pyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine (0.085 g, 0.233 mmol), 3,3-difluoropyrrolidine HCl (0.100 g, 0.699 mmol), pd2(dba)3 (10.67 mg, 0.012 mmol), and 2-(dicyclohexylphosphino)-2′-(n,n-dimethylamino)biphenyl (0.014 g, 0.035 mmol) was added 1.0 M lithium bis(trimethylsilyl)amide (1.398 mL, 1.398 mmol) in THF and the resulting mixture was heated at 90° C. for 17 h. The mixture was concentrated and purified by reverse phase HPLC to afford (S)-3-(3,3-difluoropyrrolidin-1-yl)-7-(pyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-fa09d4e3b55c4240b703d5b6df481d62
Source noteuspto-grants-2014_11