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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130509Generated: October 31, 2026

Pyridine → HCID 66628528, compound

https://huagongshe.com/reaction/130509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium ChlorideHCID 5234—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
ReactantHCID 66628652HCID 66628652—
SolventChloroformHCID 6212—
ProductHCID 66628528HCID 6662852839.3%

Reaction Steps

42 μL of pyridine and 123 mg of 3,4-dichlorobenzylbromide were added to 175 mg of (1R,2R,3R,5R,6R)-3-amino-2-t-butoxycarbonylamino-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester dissolved in 0.88 mL of chloroform at ice-cooling, and then the mixture was stirred for 3 days at room temperature. A saturated aqueous solution of sodium chloride was added thereto, and the mixture was extracted five times with chloroform. The organic layers were combined and then dried over anhydrous sodium sulfate. The desiccant was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel: Wako gel C200 (made by Wako Pure Chemical Industries Ltd.), eluent: chloroform-ethanol=100:1 to 50:1, followed by hexane-ethyl acetate=5:1), thereby yielding 98 mg of (1R,2R,3R,5R,6R)-2-t-butoxycarbonylamino-3-(3,4-dichlorobenzylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381746B2
Source datasetuspto-grants-2008_06
ORD IDord-2f43361447674f879991c1fd1af02e31
Source noteuspto-grants-2008_06