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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911474Generated: November 1, 2026

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

https://huagongshe.com/reaction/1911474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Propan-2-yl)-1,4-diazepaneHCID 12236513—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-propan-2-yl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 6658980379.3%

Reaction Steps

A solution of methyl 2-chloropyrimidine-5-carboxylate (209 mg, 1.21 mmol) in dichloromethane (4.00 ml) was added to a stirred solution of 1-propan-2-yl-1,4-diazepane (172 mg, 1.21 mmol) and N-ethyl-N-propan-2-ylpropan-2-amine (0.523 ml, 3.02 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-propan-2-yl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (267 mg, 79%) 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-c9876070fde24f29aa83b8807c175de6
Source noteuspto-grants-2013_12