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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911479Generated: November 2, 2026

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

https://huagongshe.com/reaction/1911479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-MethylhomopiperazineHCID 228349—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-methyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 6658965494.4%

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-methyl-1,4-diazepane (0.144 mL, 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-methyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (274 mg, 94%) as a white solid. 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-640332dc9a7f4506be99bcc8538a6698
Source noteuspto-grants-2013_12