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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214980Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-Amino-4-[4-(2-methoxyethoxy)phenyl]-6-({[2-(4-morpholinyl)-1,3-thiazol-4-yl]-methyl}sulphanyl)pyridine-3,5-dicarbonitrile

https://huagongshe.com/reaction/2214980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 15290886HCID 15290886—
ReactantHCID 178496105HCID 178496105—
SolventDimethylformamideHCID 6228—
Product2-Amino-4-[4-(2-methoxyethoxy)phenyl]-6-({[2-(4-morpholinyl)-1,3-thiazol-4-yl]-methyl}sulphanyl)pyridine-3,5-dicarbonitrileHCID 21949077—

Reaction Steps

2 g (6.13 mmol) of 2-amino-4-[4-(2-methoxyethoxy)phenyl]-6-sulphanylpyridine-3,5-dicarbonitrile and 2.68 g (12.26 mmol) of 4-(4-(chloromethyl)-1,3-thiazol-2-yl]morpholine are dissolved in dry DMF (50 ml), and 1.83 ml (12.26 mmol) of DBU are added. After 3 hours of stirring at RT, the solvent is removed using a rotary evaporator and the residue is purified by preparative HPLC (column: Kromasil 100 C18 250×20 mm, 10 μm; acetonitrile/water gradient: 3 minutes of 10% acetonitrile which is then, over a period of 30 minutes, increased to 80% acetonitrile; flow rate: 25 ml/min). This gives 1.70 g (55% of theory) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109218B2
Source datasetuspto-grants-2006_09
ORD IDord-0330e59f24904136ab879f6c6fa678e4
Source noteuspto-grants-2006_09