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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092178Generated: October 26, 2026

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

https://huagongshe.com/reaction/1092178

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 numberUS08129391B2
Source datasetuspto-grants-2012_03
ORD IDord-264fe19a92b842c898d47882f78cdec6
Source noteuspto-grants-2012_03