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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380848Generated: October 31, 2026

Pyridine → HCID 66628528, compound

https://huagongshe.com/reaction/2380848

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-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester dissolved in 0.88 mL of chloroform at ice-cooling, and 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. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel: Wako gel C200, 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-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258133B2
Source datasetuspto-grants-2012_09
ORD IDord-d54321262bb04fd78cdde77e25b546e8
Source noteuspto-grants-2012_09