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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783413Generated: October 29, 2026

Diisopropylethylamine → 5-Chloro-thiophene-2-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-amide

https://huagongshe.com/reaction/1783413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant[(R)-1-(2,4-Dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-carbamic acid tert-butyl esterHCID 57589908—
SolventDichloromethaneHCID 6344—
Product5-Chloro-thiophene-2-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-amideHCID 86610743—

Reaction Steps

[(R)-1-(2,4-Dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-carbamic acid tert-butyl ester (0.85 g, 1.85 mmol) was dissolved in 38 ml dichloromethane. 4 M HCl/1,4-dioxan (20 ml) were added dropwise and the mixture was allowed to react for 1 h. The reaction mixture was concentrated under reduced pressure and concentrated once from acetonitrile. To 291 mg of the resultant hydrochloride salt was added CH2Cl2 (20 ml) followed by the dropwise addition of Hünig's base (0.36 ml, 2.1 mmol). A solution of 5-chlorothiophene-2-sulfonyl chloride (0.21 g, 0.9 mmol) in CH2Cl2 (5 ml) was added and the reaction mixture (pH 8) was stirred for a further 1.5 h. The reaction mixture was purified over silica gel (heptane-ethylacetate, 95:5-0:100): white solid 0.40 g (97%);.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501406B2
Source datasetuspto-grants-2009_03
ORD IDord-0ee4173d9ead4250a3904aea770d4184
Source noteuspto-grants-2009_03