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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897321Generated: October 28, 2026

Dimethylamine → HCID 22346324, compound

https://huagongshe.com/reaction/897321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantHCID 22346362HCID 22346362—
SolventDichloromethaneHCID 6344—
ProductHCID 22346324HCID 22346324—

Reaction Steps

To a solution of N-(4-fluorobenzyl)-8-methoxy-5-(methylamino)-1,6-naphthyridine-7-carboxamide(93 mg, 0.27 mmol) in CH2Cl2 (1 mL) at OC was added diisopropylethylamine (0.14 mL, 1.5 mmol) and triphosgene (0.04 g, 0.14 mmol) and the mixture was stirred at room temperature for 16 hr. Additional diisopropylethylamine (0.07 mL, 0.08 mmol) and triphosgene (0.02 g, 0.07 mmol) was added and the reaction was stirred an additional 16 hr at room temperature. A portion of this solution (0.5 mL) was treated with dimethylamine (0.41 mL of a 2M solution in THF, 0.82 mmol). The solvent was evaporated in vacuo and the residue dissolved in DMF (1 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 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-9d95ff91090e4e6f95a3d2be85c6a5dc
Source noteuspto-grants-2005_07