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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388016Generated: November 2, 2026

1,3-Bis(benzyloxycarbonyl)-2-methylisothiourea → HCID 178432740, compound

https://huagongshe.com/reaction/2388016

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Bis(benzyloxycarbonyl)-2-methylisothioureaHCID 4664213—
ReactantTert-butyl [3-(5-amino-6-methylpyridin-3-yl)propyl]carbamateHCID 68222687—
CatalystMercuric ChlorideHCID 24085—
SolventDichloromethaneHCID 6344—
ProductHCID 178432740HCID 17843274061%

Reaction Steps

To a solution of tert-butyl [3-(5-amino-6-methylpyridin-3-yl)propyl]carbamate (2.99 g, 11.3 mmol), 1,3,-bis(benzyloxycarbonyl)-2-methyl-2-thiopseudourea (3.41 g, 9.51 mmol), and mercury(II) chloride (3.37 g, 12.4 mmol) in DCM (100 mL) was added TEA (5.19 mL, 37.3 mmol) dropwise via syringe. The reaction mixture was allowed to stir at rt overnight. The reaction mixture was filtered over a pad of Celite® and the resulting filtrate was concentrated. The residue was purified by column chromatography to give dibenzyl {(Z)-[(5-{3-[(tert-butoxycarbonyl)amino]propyl}-2-methylpyridin-3-yl)amino]methylylidene}biscarbamate (3.34 g, 61%) as a white solid. LCMS (FA): Rt=1.90 min, m/z=576.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268992B2
Source datasetuspto-grants-2012_09
ORD IDord-095228c6e35f4a63b9fef7e1587790f3
Source noteuspto-grants-2012_09