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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371305Generated: October 26, 2026

Benzyl chloroformate → (7S,10S,13S)-13-Benzyloxycarbonylamino-10-isobutyl-9,12-dioxo-2-oxa-8,11-diaza-bicyclo-[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2371305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 86650239HCID 86650239—
SolventDimethylformamideHCID 6228—
Product(7S,10S,13S)-13-Benzyloxycarbonylamino-10-isobutyl-9,12-dioxo-2-oxa-8,11-diaza-bicyclo-[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl esterHCID 44191155—

Reaction Steps

Amine 6 (4.00 g, 8.78 mmol) was dissolved in anhydrous DMF (30 mL). Benzyl chloroformate (1.88 mL, 13.2 mmol) and DIPEA (6.11 mL, 35.1 mmol) were added and the reaction mixture was stirred at rt for 18 h before being partitioned between chloroform and 1M hydrochloric acid. The aqueous phase was extracted three more times with chloroform and the combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. Purification was achieved using flash chromatography, eluting with a gradient of 15% EtOAc/DCM to 50% EtOAc/DCM to yield an off-white solid, 2.10 g, 43%. Rf=0.43 (30% EtOAc/DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710178B2
Source datasetuspto-grants-2014_04
ORD IDord-3f0e2efc4d9f432183a775ac7d642722
Source noteuspto-grants-2014_04