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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428003Generated: October 31, 2026

Diisopropylethylamine → HCID 66647723, compound

https://huagongshe.com/reaction/2428003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(+-)-2-(Aminomethyl)-1-N-Boc-pyrrolidineHCID 2756484—
ReactantEthyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylateHCID 57474573—
ReactantHCID 86627719HCID 86627719—
SolventDimethylformamideHCID 6228—
ProductHCID 66647723HCID 6664772395%

Reaction Steps

(S)-Ethyl 2-((1-(tert-butoxycarbonyl)pyrrolidin-2-yl)methylamino)-6-(2-methoxy-phenylamino)-5-nitropyrimidine-4-carboxylate. Ethyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate (See Example 30.A) (0.300 g, 0.852 mmol), (S) 1-boc-(aminomethyl)pyrrolidine (0.206 g, 1.02 mmol) and diisopropylethylamine (0.164 g, 1.27 mmol.) 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 (0.416 g, 95%). MS (ESI) m/z 517.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968556B2
Source datasetuspto-grants-2011_06
ORD IDord-15605303b5c74138ab8a0426eea1494c
Source noteuspto-grants-2011_06