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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916336Generated: November 2, 2026

3-((Tert-butyldimethylsilyl)oxy)propanal → (RS)-1-[([3-(tert-butyl-dimethyl-silanyloxy)-propy]-{2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethyl}-amino)-methyl]-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-one

https://huagongshe.com/reaction/1916336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—
Reactant(1RS)-9-fluoro-1-({2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethylamino}-methyl)-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 67348543—
Product(RS)-1-[([3-(tert-butyl-dimethyl-silanyloxy)-propy]-{2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethyl}-amino)-methyl]-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 6713443287%

Reaction Steps

Starting from the compound of Example 4 and 3-(tert-butyldimethylsilyloxy)-propionaldehyde and using procedure E, the title compound was obtained as a yellow foam (82 mg; 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618092B2
Source datasetuspto-grants-2013_12
ORD IDord-aa5ba6672bc04ea6aafb2a11ea50588f
Source noteuspto-grants-2013_12