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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916337Generated: October 31, 2026

2-((Tert-butyldimethylsilyl)oxy)acetaldehyde → (RS)-1-[([2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-{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/1916337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
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-[([2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-{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 6735260959%

Reaction Steps

Starting from the compound of Example 4 and tert-butyldimethylsilyloxy-acetaldehyde and using procedure E, the title compound was obtained as a yellow foam (55 mg; 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618092B2
Source datasetuspto-grants-2013_12
ORD IDord-feaa69128dea42749eddcaaad7c77f1c
Source noteuspto-grants-2013_12