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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655783Generated: October 30, 2026

Hydrochloric Acid → Methyl 2-chloro-4-[4-(piperidin-1-yl)pyrimidin-2-yl]-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/655783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 2-amino-4-[4-(piperidin-1-yl)pyrimidin-2-yl]-1,3-thiazole-5-carboxylateHCID 59402564—
SolventWaterHCID 962—
ProductMethyl 2-chloro-4-[4-(piperidin-1-yl)pyrimidin-2-yl]-1,3-thiazole-5-carboxylateHCID 5940252454%

Reaction Steps

To a stirred solution of methyl 2-amino-4-[4-(piperidin-1-yl)pyrimidin-2-yl]-1,3-thiazole-5-carboxylate (Intermediate 62, 0.070 g, 0.219 mmol) in concentrated HCl (1 mL), sodium nitrite (0.045 g, 0.658 mmol) in water (1 mL) was added drop wise at 0° C. The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was cooled to 5-10° C. and basified with saturated sodium bicarbonate solution (20 mL). The aqueous layer was extracted with ethyl acetate (2×30 mL). The combined organic layer was washed with brine solution, dried and concentrated under reduced pressure to obtain methyl 2-chloro-4-[4-(piperidin-1-yl)pyrimidin-2-yl]-1,3-thiazole-5-carboxylate 0.040 g (54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071605B2
Source datasetuspto-grants-2011_12
ORD IDord-bd6eb21a19dd4eb98daeceaae575a2ac
Source noteuspto-grants-2011_12