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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389756Generated: October 27, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → tert-Butyl {2-[(5-cyanopyridin-2-yl)thio]ethyl}carbamate

https://huagongshe.com/reaction/2389756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantN-(tert-butoxycarbonyl)-2-aminoethanethiolHCID 3017761—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl {2-[(5-cyanopyridin-2-yl)thio]ethyl}carbamateHCID 59313027—

Reaction Steps

2-Chloro-5-cyanopyridine (500 mg, 3.6 mmol), tert-butyl (2-mercaptoethyl)carbamate (426 mg, 2.4 mmol) and 1,8-diazabicyclo(5.4.0)undec-7-ene (549 mg, 3.6 mmol) are dissolved in DMF (5 ml) and stirred at RT under argon for 12 h. The reaction mixture is diluted with water (100 ml) and extracted with ethyl acetate (3×75 ml). The combined organic phases are washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and concentrated. After removal of the solvent, the residue is purified by preparative RP-HPLC (gradient of eluent: water/acetonitrile 90:10 to 10:90). 612 mg (91% of theory) of the product are obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273752B2
Source datasetuspto-grants-2012_09
ORD IDord-d83be4cae71c4cd98ed06de31c4e6aaa
Source noteuspto-grants-2012_09