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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427991Generated: October 25, 2026

Diisopropylethylamine → HCID 178489571, compound

https://huagongshe.com/reaction/2427991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylateHCID 57474573—
ReactantHCID 178470296HCID 178470296—
ReactantHCID 178511715HCID 178511715—
SolventDimethylformamideHCID 6228—
ProductHCID 178489571HCID 17848957182%

Reaction Steps

Ethyl 2-(trans-4-hydroxycyclohexylamino)-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate. Ethyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate (See Example 30.A) (0.300 g, 0.852 mmol), trans-4-aminocyclohexanol (0.117 g, 1.022 mmol) and diisopropylethylamine were reacted according to General Procedure C, except at room temperature and in dimethylformamide (5 mL). The crude reaction mixture was condensed and purified using Biotage chromatography (0-100% ethyl acetate in hexanes) to afford the title compound (0.303 g, 82%). MS (ESI) m/z 432.5 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968556B2
Source datasetuspto-grants-2011_06
ORD IDord-7196577e2778472cbcb087241446bde8
Source noteuspto-grants-2011_06