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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911481Generated: October 26, 2026

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

https://huagongshe.com/reaction/1911481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
Reactant1-Cyclopropylhexahydro-1H-1,4-diazepineHCID 20348476—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 6658997497.3%

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-cyclopropyl-1,4-diazepane (247 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-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (312 mg, 97%) as a cream 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-cfd07455b8444d99aa64bd50d860f79c
Source noteuspto-grants-2013_12