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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875562Generated: October 31, 2026

Methyl iodide → HCID 91084433, compound

https://huagongshe.com/reaction/1875562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantBenzoic acid, 2-amino-5-iodo-HCID 72911—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
ReactantHCID 22619321HCID 22619321—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 91084433HCID 9108443374.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

The mixture of N-(t-butoxycarbonyl)-4-amino-L-phenylalanine methylester (10.25 g), 2-amino-5-iodobenzoic acid (9.18 g), EDC/HCl (6.8 g), HOBT (4.8 g), triethylamine (6.6 mL) and tetrahydrofuran (300 mL) was stirred at 40° C. overnight. The solution wherein about a half amount of the solvent was removed was diluted with water and ethyl acetate and liquid separation was conducted. The organic layer was washed with water, saturated aqueous solution of ammonium chloride, saturated aqueous solution of sodium hydrogen carbonate and saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was removed to obtain 22 g of the crude material. The crude material (22 g), CDI (carbonyldiimidazole) (17 g) and DMF (200 mL) were stirred at 80° C. overnight. The reaction solution was diluted with water and ethyl acetate, and liquid separation was conducted. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was removed to obtain 23.4 g of the crude material. The crude material (23.4 g), methyl iodide (3 mL), potassium carbonate (10.0 g) and DMF (100 mL) were stirred at room temperature overnight. The reaction solution was diluted with water and ethyl acetate, and liquid separation was conducted. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was removed to obtain 15 g of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309561B2
Source datasetuspto-grants-2012_11
ORD IDord-0fb07489055c4942b653f73549d909e2
Source noteuspto-grants-2012_11