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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425451Generated: October 28, 2026

Dimethylamine → HCID 67243468, compound

https://huagongshe.com/reaction/2425451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantHCID 67243714HCID 67243714—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67243468HCID 67243468—

Reaction Steps

A solution of (S)-3-[2-(2-bromoethoxy)acetyl]amino-1-(tert-butoxycarbonyl)pyrrolidine (195 mg) prepared in Step C in tetrahydrofuran (2 ml) was added with dimethylamine (2 M solution in tetrahydrofuran, 4.5 ml, Aldrich) at 0° C., and the mixture was stirred at room temperature for 23 hours. The volatile components were evaporated under reduced pressure, and the residue was added with saturated aqueous sodium hydrogencarbonate, and extracted five times with chloroform. The combined organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain the title compound (180 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964613B2
Source datasetuspto-grants-2011_06
ORD IDord-11bfc50c08b14f45aa61c9a8dc0a7800
Source noteuspto-grants-2011_06