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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091926Generated: October 26, 2026

Water → (1S)-(2,4-Dichloro-6-methyl-pyrimidin-5-ylmethyl)methyl-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amine

https://huagongshe.com/reaction/1091926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(1S)-1,2,3,4-Tetrahydro-N-methyl-1-naphthalenamineHCID 7128547—
Reactant2,4-Dichloro-5-(chloromethyl)-6-methylpyrimidineHCID 13568282—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product(1S)-(2,4-Dichloro-6-methyl-pyrimidin-5-ylmethyl)methyl-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amineHCID 57531525—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a flask containing 2,4-dichloro-5-chloromethyl-6-methyl-pyrimidine (107 mg, 0.51 mmol) in absolute ETOH (10 mL) is added K2CO3 (70 mg, 1.0 eq., 0.51 mmol) and the reaction is cooled to 0° C. with an ice bath. (1S)-Methyl-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amine (82 mg, 1.0 equiv, 0.51 mmol) in 1.0 mL of EtOH is added via syringe in one portion and allowed to warm to ambient temperature over 3 h. Water (50 mL) and EtOAc (50 mL) is added and the EtOAc layer is washed with water (100 mL) and brine (50 mL) and dried over Na2SO4. Concentration and vacuum drying affords the title compound as a yellow gum. [mass expected (336.26); mass found (336.30)]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129395B2
Source datasetuspto-grants-2012_03
ORD IDord-c5bd1308cbcd4e70ba99e17e5006362c
Source noteuspto-grants-2012_03