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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036793Generated: November 3, 2026

Glycine ethyl ester → HCID 61795720, compound

https://huagongshe.com/reaction/2036793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine ethyl esterHCID 12176—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromopyridine-3-sulfonyl chlorideHCID 20324474—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61795720HCID 6179572014%

Reaction Steps

A solution of 5-bromopyridine-3-sulfonyl chloride (3.5 g, 14 mmol) (described in the synthesis of Example 170) and glycine ethylester (2.1 g, 20 mmol), diisopropyl ethyl amine (2.6 g, 20 mmol) in THF (70 mL) was stirred at room temperature for 16 h. The reaction mixture was partitioned between saturated aqueous sodium chloride and ethyl acetate. The organic solution was separated, dried and evaporated under reduced pressure. The residue was purified using flash column chromatography using ethyl acetate/hexanes as eluent to obtain ethyl 2-(5-bromopyridine-3-sulfonamido)acetate (600 mg, 14%). LCMS Method I: retention time 1.31 min; [M+1]=323, 325.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-dc4d0cc30379421e8a627a0edc169eb2
Source noteuspto-grants-2013_11