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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911470Generated: October 27, 2026

Diisopropylethylamine → Methyl 2-(4-ethyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1911470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Ethyl-1,4-diazepaneHCID 7577538—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-ethyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 6658995987.4%

Reaction Steps

A solution of methyl 2-chloropyrimidine-5-carboxylate (200 mg, 1.16 mmol) in dichloromethane (4.00 mL) was added to a stirred solution of 1-ethyl-1,4-diazepane (149 mg, 1.16 mmol) and N-ethyl-N-propan-2-ylpropan-2-amine (0.902 mL, 5.22 mmol) in dichloromethane (4.00 mL) at 25° C. The resulting solution was stirred at ambient temperature for 18 h. The reaction mixture was evaporated to dryness and redissolved in MeOH (20 mL) and the crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and evaporated to dryness to afford methyl 2-(4-ethyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (268 mg, 87%) as a cream oil which crystallised on standing. This was used directly with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-e5aa80c8ed514a9abcd444ceab0e3857
Source noteuspto-grants-2013_12