Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897323Generated: October 29, 2026

Diisopropylethylamine → HCID 22346264, compound

https://huagongshe.com/reaction/897323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant2-MorpholinoethylamineHCID 408285—
ReactantHCID 22346362HCID 22346362—
SolventDichloromethaneHCID 6344—
ProductHCID 22346264HCID 22346264—

Reaction Steps

To a solution of N-(4-fluorobenzyl)-8-methoxy-5-(methylamino)-1,6-naphthyridine-7-carboxamide (504 mg, 1.48 mmol) in CH2Cl2 (5 mL) at OC was added diisopropylethylamine (0.77 mL, 4.4 mmol) and triphosgene (0.22 g, 0.74 mmol) and the mixture was stirred at room temperature for 16 hr. Additional diisopropylethylamine (0.77 mL, 4.4 mmol) and triphosgene (0.22 g, 0.74 mmol) was added and the reaction was stirred an additional 16 hr at room temperature. The reaction was diluted with CH2Cl2 and a portion of this solution (1.0 mL) was treated with 2-morpholinoethylamine (0.12 mL 0.89 mmol) at room temperature for 16 hr. The solvent was evaporated in vacuo and the residue dissolved in DMSO (0.5 mL) and purified by reverse phase HPLC. (Vydak C18, Gradient elution with Water:Acetonitrile 95:5 to 5:95 with 0.1% TFA at 30 mL/min over 15 mins). Lyophilization of the pure fractions afforded the title compound as an off white solid which was used directly in step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-12d00f3e82e94fde9c26af620a0c2a68
Source noteuspto-grants-2005_07