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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10072Generated: October 28, 2026

Methyl iodide → Methyl 4'-[({[1-(methylamino)cyclo-propyl]carbonyl}amino)methyl]-1,1'-biphenyl-2-carboxylate

https://huagongshe.com/reaction/10072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4'-({[(1-aminocyclopropyl)carbonyl]amino}methyl)-1,1'-biphenyl-2-carboxylateHCID 21988955—
SolventDichloromethaneHCID 6344—
ProductMethyl 4'-[({[1-(methylamino)cyclo-propyl]carbonyl}amino)methyl]-1,1'-biphenyl-2-carboxylateHCID 2198895334.8%

Reaction Steps

Methyl 4′-({[(1-aminocyclopropyl)carbonyl]amino}methyl)-1,1′-biphenyl-2-carboxylate (200 mg, 0.62 mmol), prepared according to Example 1, was dissolved in 5 mL of DCM along with iodomethane (130 mg, 0.93 mmol) and triethylamine (75 mg, 0.74 mmol). After no reaction was observed at ambient temperature, the reaction mixture was heated to reflux for about two days. After the first day, additional iodomethane was added (ca. 3–5 equiv.). After two days >50% of the starting material was consumed. The reaction mixture was concentrated under reduced pressure and the residue was subjected to silica gel chromatography eluting with 1–10% MeOH in DCM to afford 73 mg of methyl 4′-[({[1-(methylamino)cyclo-propyl]carbonyl}amino)methyl]-1,1′-biphenyl-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091380B2
Source datasetuspto-grants-2006_08
ORD IDord-ea24b883e61146ae966eb07d2c1926f9
Source noteuspto-grants-2006_08