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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389644Generated: October 30, 2026

Diisopropylethylamine → 5-Chloro-thiophene-2-carboxylic acid [(S)-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-3-((S)-3-methyl-morpholin-4-yl)-3-oxo-propyl]-amide

https://huagongshe.com/reaction/389644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-thiophene-2-carboxylic acid [(S)-2-amino-3-((S)-3-methyl-morpholin-4-yl)-3-oxo-propyl]-amideHCID 67155248—
Reactant2-Ethyl-3-(3-oxomorpholino)benzene-1-sulfonyl chlorideHCID 72792889—
SolventDichloromethaneHCID 6344—
Product5-Chloro-thiophene-2-carboxylic acid [(S)-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-3-((S)-3-methyl-morpholin-4-yl)-3-oxo-propyl]-amideHCID 44200855—

Reaction Steps

5-Chloro-thiophene-2-carboxylic acid [(S)-2-amino-3-((S)-3-methyl-morpholin-4-yl)-3-oxo-propyl]-amide, Intermediate 3 (95 mg, 0.287 mmol) was dissolved in 2 ml DCM and DIPEA (151 μl, 0.861 mmol). 2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonyl chloride, Intermediate 7 (91 mg, 0.3 mmol) in 2 ml DCM was slowly added and the reaction was stirred for 75 min. After that the solution was evaporated to dryness and purified by prep. HPLC. After lyophilization the title compound was obtained as colorless, amorphous solid. Yield: 108 mg, 63%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378092B2
Source datasetuspto-grants-2013_02
ORD IDord-60fc9bf5f8064fc0a10549b3ec2b68fc
Source noteuspto-grants-2013_02