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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515953Generated: October 25, 2026

Triethylamine → Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/515953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protectedHCID 1514389—
ReactantMethyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 58317549—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductMethyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 6723801562.2%

Reaction Steps

A solution of methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (1.2 g, 4.11 mmol), tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (0.882 g, 4.11 mmol) and triethylamine (1.720 mL, 12.34 mmol) in DMA (10 mL) was heated at 90° C. for 4 h. The solution was then diluted with EtOAc, washed with brine and water. The organic extract was dried and concentrated under reduced pressure to give a light yellow residue; white crystals were formed upon triturating with ACN (5 mL). The resultant solid was filtered, washed with ACN, and dried to give the title compound as white solid (1.2 g, 62%). [M+H] calc'd for C25H35N5O4, 470; found, 470.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108970B2
Source datasetuspto-grants-2015_08
ORD IDord-805520152a0b406485e703eae335253d
Source noteuspto-grants-2015_08