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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548934Generated: October 30, 2026

4,6-Dichloropyrimidine → HCID 58940650, compound

https://huagongshe.com/reaction/548934

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-DichloropyrimidineHCID 70943—
Reactanttert-Butyl azetidin-3-yl(methyl)carbamateHCID 23033645—
SolventIsopropanolHCID 3776—
ProductHCID 58940650HCID 5894065064.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Azetidin-3-yl-methyl-carbamic acid tert-butyl ester (1.97 g, 11 mmol) in IPA (5 mL) was added dropwise to a stirred solution of 4,6-dichloropyrimidine (1.49 g, 10 mmol) in IPA (20 mL) followed by dropwise addition of TEA (2.11 mL, 15.1 mmol) at ambient temperature under N2. The resulting milky yellow solution was heated to 80° C. and maintained at 80° C. for 2 hours. The solution was allowed to cool and evaporated to give a yellow oil. The crude material was partitioned between DCM (70 mL) and water (30 aqueous extract was re-extracted with DCM (70 mL). The combined organic extract was washed with saturated aqueous sodium bicarbonate (30 mL), dried (MgSO4), filtered and evaporated to give a coloured oil. The crude oil was purified by flash column chromatography on silica gel eluting with DCM:MeOH (99:1 changing to 96:4 by volume) to yield the title compound as a solid (1.93 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943628B2
Source datasetuspto-grants-2011_05
ORD IDord-2b3e615683a543daaedf44ac0c9895af
Source noteuspto-grants-2011_05