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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371318Generated: October 31, 2026

Benzyl chloroformate → (9R,12S,15S)-15-Benzyloxycarbonylamino-12-isopropyl-11,14-dioxo-2-oxa-7-thia-10,13-diaza-bicyclo[15.2.2]henicosa-1(20),17(21),18-triene-9-carboxylic acid methyl ester

https://huagongshe.com/reaction/2371318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantDichloromethane ethylacetateHCID 21226138—
Reactant(9R,12S,15S)-15-Amino-12-isopropyl-11,14-dioxo-2-oxa-7-thia-10,13-diaza-bicyclo-[15.2.2]-henicosa-1(20),17(21),18-triene-9-carboxylic acid methyl ester hydrochlorideHCID 66846960—
SolventDimethylformamideHCID 6228—
Product(9R,12S,15S)-15-Benzyloxycarbonylamino-12-isopropyl-11,14-dioxo-2-oxa-7-thia-10,13-diaza-bicyclo[15.2.2]henicosa-1(20),17(21),18-triene-9-carboxylic acid methyl esterHCID 66847567—

Reaction Steps

Amine 34 (0.200 g, 0.410 mmol) was dissolved in anhydrous DMF (10 mL). Benzyl chloroformate (0.0877 mL, 0.615 mmol) and DIPEA (0.286 mL, 1.64 mmol) were added. The resultant reaction mixture was stirred at rt for 18 h before being partitioned between EtOAc and 1M hydrochloric acid. The aqueous phase was extracted twice more with EtOAc and the combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica using a gradient of EtOAc/DCM to yield an off-white solid, 0.0430 g, 18%. Rf=0.44 (30% EtOAc/DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710178B2
Source datasetuspto-grants-2014_04
ORD IDord-bb9ef048950746b780d2501f96d5c81d
Source noteuspto-grants-2014_04