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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946681Generated: November 4, 2026

Triethylamine → HCID 25183073, compound

https://huagongshe.com/reaction/1946681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Aminobenzyl alcoholHCID 69331—
Reactant6-[Cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acidHCID 59446841—
ReactantHCID 86644304HCID 86644304—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 25183073HCID 2518307372%

Reaction Steps

A solution of 6-(cyclohexyl-cyclopropylmethyl-amino)-pyrimidine-4-carboxylic acid (Intermediate 13, 1.00 g; 3.63 mmol) in dry DMF (100 ml) was treated with polymer-supported Mukaiyama reagent, prepared as described in “S. Crosignani et al. Org. Lett. 2004, 6(24), 4579-4582” (2 987 mg; 6.54 mmol), 4-aminobenzyl alcohol (Fluka, 492 mg; 3.99 mmol) and triethylamine (1.52 ml; 10.9 mmol). The reaction mixture was then stirred at room temperature for 18 hours. DCM was added and the product was filtered through an SPE column (Isolute NH2, 10 g) and the column washed with DCM. The mixture was concentrated then rediluted in AcOEt. The organic phase was washed 5 times with brine, dried over MgSO4 and the solvent removed under vacuum to give the title compound (990 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-8af2e2d7fb244f2faf0994e5cc97178b
Source noteuspto-grants-2013_03