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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746650Generated: October 31, 2026

Ammonium formate → Methyl 6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylate

https://huagongshe.com/reaction/1746650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantMethyl 2-chloro-6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylateHCID 59446993—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductMethyl 6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylateHCID 5944688997.3%

Reaction Steps

A solution of methyl 2-chloro-6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylate (Intermediate 11, 4.77 g; 14.7 mmol) in 150 ml of iPrOH was treated with 780 mg of palladium (10% on C). The suspension was degassed and a solution of ammonium formate (6.96 g; 110 mmol) in 20 ml of water was added. After stirring at RT for 45 minutes, the suspension was filtered on a pad of Celite, the remaining residue was twice rinsed with 50 ml of iPrOH and the combined filtrates were evaporated under reduced pressure. The remaining colorless residue was partitioned between 150 ml of MTBE and 150 ml of water. Both layers were separated. The organic phase was once washed with 100 ml of brine, dried over MgSO4 and concentrated under reduced pressure to give the title compound as colorless oil (4.14 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150519B2
Source datasetuspto-grants-2015_10
ORD IDord-03132e227e5a4c389063573a25948c90
Source noteuspto-grants-2015_10