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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629742Generated: October 26, 2026

1,1'-Carbonyldiimidazole → HCID 86726342, compound

https://huagongshe.com/reaction/629742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(6-Chloropyridin-2-yl)methanamineHCID 10313191—
ReactantHCID 86726337HCID 86726337—
SolventPyridineHCID 1049—
ProductHCID 86726342HCID 86726342—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of tert-Butyl (2R,5R)-2-[2-(3-{[N-(tert-butoxycarbonyl)-4-fluoro-β-(4-fluorophenyl)-L-phenylalanyl]amino}-5-fluoropyridin-4-yl)ethyl]-5-(hydroxymethyl)morpholine-4-carboxylate (Example 149, Step 7) (677 mg, 0.95 mmol) and carbonyldiimidazole (154 mg, 0.95 mmol) was added dry pyridine (22.5 mL). The resulting solution was heated at 60° C. and stirred for 2 h. This solution was then distributed in 0.5 mL (0.021 mmol) aliquots to 45 2-dram sample vials, each containing a diverse amine (0.042 mmol); among them (6-chloropyridin-2-yl)methanamine. The resulting mixtures were stirred at 60° C. for 3 h. Solvent was removed under stream of N2 gas. The residues were diluted with 4 N HCl/diethyl ether (1 mL) and stirred at room temperature for 16 h. Solvent was removed under stream of N2 gas, and the residues were diluted with DMSO and purified by mass-guided reversed-phase HPLC (10-90% CH3CN:0.1% NH4OH/H2O). HRMS (ES) 683.2353 (M+H). found, 683.2355 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-2446a8c255c64da9916cf6108b50807f
Source noteuspto-grants-2016_04