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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641141Generated: October 27, 2026

N-Hydroxysuccinimide → N-(4-Methoxy-phenyl)-N-(succinimidyl-oxycarbonyl-propyl-sulfonyl)-thieno[2,3-b]quinoline-4-carboxamide

https://huagongshe.com/reaction/641141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxysuccinimideHCID 80170—
Reactant4-(2-Isocyanoethyl)morpholineHCID 2759434—
ReactantN-(4-Methoxy-phenyl)-N-(carboxypropyl-sulfonyl)-thieno[2,3-b]quinoline-4-carboxamideHCID 68637627—
ProductN-(4-Methoxy-phenyl)-N-(succinimidyl-oxycarbonyl-propyl-sulfonyl)-thieno[2,3-b]quinoline-4-carboxamideHCID 86607522107.5%

Reaction Steps

A mixture of 66 mg (0.12 mmol) N-(4-Methoxy-phenyl)-N-(carboxypropyl-sulfonyl)-thieno[2,3-b]quinoline-4-carboxamide 17, 25 μl (0.17 mmol) 2-Morpholino-ethyl-isocyanide (MEI) and 21 mg (0.17 mmol) N-Hydroxysuccinimide (HOSu) was stirred overnight at room temperature. The solvent was removed under vacuum and the oily residue was purified by silica gel column chromatography (eluent: methylene chloride/acetone 9:1+0.1% acetic acid). The appropriate fractions were combined and evaporated to yield 75 mg of 18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07695980B2
Source datasetuspto-grants-2010_04
ORD IDord-577e719816694efea57b62b8871923ab
Source noteuspto-grants-2010_04