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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615861Generated: November 3, 2026

Diisopropylethylamine → HCID 66865455, compound

https://huagongshe.com/reaction/1615861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58118678HCID 58118678—
ReactantHCID 86650290HCID 86650290—
SolventDimethylformamideHCID 6228—
ProductHCID 66865455HCID 66865455—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of tert-butyl (8R)-8-(3,5-difluorophenyl)-8-methyl-10-oxo-9-[2-oxo-2-(pentafluorophenoxy)ethyl]-6,9-diazaspiro[4.5]decane-6-carboxylate from Step A (119 mg, 0.197 mmol), (2R)-5-hydroxy-1′-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (77 mg, 0.201 mmol, described in Intermediate 35), and N,N-diisopropylethylamine (0.17 mL, 0.98 mmol) in DMF (0.5 mL) was heated at 150° C. in a microwave reactor for 30 min. The reaction mixture was cooled and partitioned between saturated aqueous NaHCO3 (20 mL) and EtOAc (30 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified on silica gel, eluting with a gradient of hexanes:EtOAc—100:0 to 0:100, to provide the title compound. MS: m/z=803.7 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765759B2
Source datasetuspto-grants-2014_07
ORD IDord-8b8913e8cb8f4bdcb4ae5dbd3d0aa477
Source noteuspto-grants-2014_07