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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916334Generated: October 31, 2026

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

https://huagongshe.com/reaction/1916334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—
Reactant(1RS)-9-fluoro-1-(2-{[(R)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-ylmethyl]-amino}-ethyl)-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 67349051—
Product(RS)-1-(2-{[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-[2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-ylmethyl]-amino}-ethyl)-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 6734900575%

Reaction Steps

Starting from the compound of Example 10 and 3-(tert-butyldimethylsilyloxy)-propionaldehyde and using procedure E, the title compound was obtained as a colourless solid (101 mg; 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618092B2
Source datasetuspto-grants-2013_12
ORD IDord-475e4d6dba5b4d6eb76d53f4847f9c86
Source noteuspto-grants-2013_12