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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365757Generated: October 25, 2026

Dimethylformamide → 5-Chloro-7-morpholinothiazolo[5,4-d]pyrimidine-2-carbaldehyde

https://huagongshe.com/reaction/1365757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactant4-(5-Chlorothiazolo[5,4-d]pyrimidin-7-yl)morpholineHCID 57685385—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-7-morpholinothiazolo[5,4-d]pyrimidine-2-carbaldehydeHCID 57685405—

Reaction Steps

To a suspension of 4-(5-chlorothiazolo[5,4-d]pyrimidin-7-yl)morpholine 14 (1.75 g, 6.85 mmol) in dry THF at −78° C. was added a 2.5M solution of n-butyllithium (nBuLi) in hexane (3.3 mL, 1.2 eq.). After stirring for 1 h, dry DMF (796 uL, 1.5 eq.) was added. The reaction mixture was stirred for 1 h at −78° C. and then warmed slowly to room temperature. After a further 2 h at room temperature the reaction mixture was poured onto ice/water yielding a yellow precipitate. This was collected by filtration and air-dried to yield 5-chloro-7-morpholinothiazolo[5,4-d]pyrimidine-2-carbaldehyde 44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893059B2
Source datasetuspto-grants-2011_02
ORD IDord-dafaa15cf0d742e39e6ba4176b20ab22
Source noteuspto-grants-2011_02