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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969929Generated: October 30, 2026

4-Nitrophenyl chloroformate → HCID 58557070, compound

https://huagongshe.com/reaction/1969929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 67999683HCID 67999683—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventHCID 58558041HCID 58558041—
ProductHCID 58557070HCID 58557070—

Reaction Steps

To a scalemic mixture enriched in (1S,3R,4S)-3-ethyl-4-(6-tosyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)cyclopentanol (6.11 g, 14.4 mmol) in pyridine (100 mL) was added DMAP (1.93 g, 15.8 mmol) and 4-nitrophenyl carbonochloridate (4.34 g, 21.5 mmol). The resulting mixture was stirred at ambient temperature for about 3.5 h and heated at about 33° C. for about 1 h. The solid was filtered off and washed with EtOAc (30 mL). The filtrated was concd under reduced pressure. The residue was purified using silica gel chromatography eluting with 0-30% EtOAc in heptane to give a scalemic mixture enriched in (1S,3R,4S)-3-ethyl-4-(6-tosyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)cyclopentyl 4-nitrophenyl carbonate (6.63, 78%). LC/MS (Table 1, Method b) Rt=2.65 min; MS m/z: 591 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-59d19912a91749b3b5e66804de6aec8e
Source noteuspto-grants-2013_04