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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335729Generated: October 30, 2026

Lithium Hexamethyldisilazide → HCID 67241769, compound

https://huagongshe.com/reaction/335729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant2,2-DimethylmorpholineHCID 18959674—
ReactantHCID 58466124HCID 58466124—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 67241769HCID 67241769—

Reaction Conditions

Temperature110 °C

Reaction Steps

A 2-5 ml microwave vial was charged with (S)-2-amino-2′-bromo-5H-spiro[oxazole-4,9′-xanthen]-7′-ol (300 mg, 0.864 mmol) (104780-26-0), Pd2dba3 (39.6 mg, 0.043 mmol), 2′-(dicyclohexylphosphino)-N,N-dimethylbiphenyl-2-amine (40.8 mg, 0.104 mmol) and 2,2-dimethylmorpholine (299 mg, 2.59 mmol). The mixture was capped with argon and LiHMDS (1M in THF) (4321 μL, 4.32 mmol) was added and the vial was sealed and heated at 110° C. in microwave reactor for 1 hr. The reaction mixture was quenched by addition of 2 ml water and EtOAc, then saturated NH4Cl was added. The organic layer was filterd through Celite, concentrated in vacuo and purified on a 40 g RediSep column using 15-80% DCM/MeOH/NH4OH in DCM to afford (R)-2-amino-2′-(2,2-dimethylmorpholino)-5H-spiro[oxazole-4,9′-xanthen]-7′-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-11a4d7484b7c4bde937c366c4fab5959
Source noteuspto-grants-2014_11