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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18039Generated: October 25, 2026

Trimethylsilyl iodide → (+/-)-cis-1-(Acetyloxy)-6methoxy-3,3,14-trimethyl-7-oxo-2,3,7,14-tetrahydro-1h-benzo[b]chromeno[6,5-g][1,8]naphthyridin-2-yl aminoacetate

https://huagongshe.com/reaction/18039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant(+/-)-cis-1-(Acetyloxy)-6-methoxy-3,3,14-trimethyl-7-oxo-2,3,7,14-tetrahydro-1h-benzo[b]chromeno[6,5-g][1,8]naphthyridin-2-yl [(tert-butoxycarbonyl)amino]acetateHCID 91322932—
SolventChloroformHCID 6212—
Product(+/-)-cis-1-(Acetyloxy)-6methoxy-3,3,14-trimethyl-7-oxo-2,3,7,14-tetrahydro-1h-benzo[b]chromeno[6,5-g][1,8]naphthyridin-2-yl aminoacetateHCID 68585121—

Reaction Steps

Add 0.14 μl of iodotrimethylsilane to a solution, at ambient temperature, of 0.1 mmol of the compound of Example 10 in 1 ml of chloroform. The reaction mixture is stirred for 5 min. at ambient temperature and then evaporated to dryness under reduced pressure. Chromatography on silica gel (dichloromethane/methanol:85/15) allows the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741325B2
Source datasetuspto-grants-2010_06
ORD IDord-f38be1e437c248a88931ebf242c1bcb4
Source noteuspto-grants-2010_06