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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391664Generated: October 29, 2026

Diisopropylethylamine → HCID 66647786, compound

https://huagongshe.com/reaction/391664

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 86627715HCID 86627715—
SolventDimethylformamideHCID 6228—
ProductHCID 66647786HCID 6664778697%

Reaction Steps

(R)-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), (R) 1-boc-(aminomethyl)pyrrolidine (0.207 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 (0.430 g, 97%). MS (ESI) m/z 517.5 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383634B2
Source datasetuspto-grants-2013_02
ORD IDord-5969bc21135d43d18b69aeff6e6de82a
Source noteuspto-grants-2013_02