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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58346Generated: October 30, 2026

1,1'-Carbonyldiimidazole → (3-{[(1-{[(Tert-butoxycarbonyl)(methyl)amino]methyl}cyclopropyl)carbonyl]amino}-propyl)(triphenyl)phosphonium bromide

https://huagongshe.com/reaction/58346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 60034817HCID 60034817—
ReactantHCID 178419277HCID 178419277—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(3-{[(1-{[(Tert-butoxycarbonyl)(methyl)amino]methyl}cyclopropyl)carbonyl]amino}-propyl)(triphenyl)phosphonium bromideHCID 8946295944.2%

Reaction Steps

1-{[(tert-butoxycarbonyl)(methyl)amino]methyl}cyclopropanecarboxylic acid (680 mg, 3.0 mmol) was dissolved in N,N-dimethylformamide (6.8 mL) and treated with N,N-carbonyldiimidazole (571 mg, 3.52 mmol). The mixture was stirred at room temperature for 30 minutes. To the solution was added (3-ammoniopropyl)(triphenyl)phosphonium dibromide (1.93 g, 4.00 mmol). The mixture was stirred overnight at room temperature and then diluted with methylene chloride and washed with 5% aqueous lithium chloride (3 times), 1N aqueous hydrogen chloride, and saturated sodium bicarbonate. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated to give crude title compound. The crude product was purified on a silica gel column eluting with a gradient of 0-20% methanol with methylene chloride to isolate the title compound (810 mg, 40%, 91% pure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434753B2
Source datasetuspto-grants-2016_09
ORD IDord-ef6fa86c78904968a31e557adb630308
Source noteuspto-grants-2016_09