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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907043Generated: November 3, 2026

Hydrochloric Acid → Boc-Gly Rotigotine

https://huagongshe.com/reaction/1907043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantRotigotine hydrochlorideHCID 180335—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductBoc-Gly RotigotineHCID 131730238—

Reaction Steps

Rotigotine HCl (1.2 g, 3.41 mmol) and Boc-Glycine-OH (1.195 g, 6.82 mmol) were dissolved in dichloromethane (150 ml) to give a suspension. After addition of DMAP (0.625 g, 5.11 mmol) and DCC (1.407 g, 6.82 mmol), the mixture was stirred for 16 hours at room temperature. The mixture was filtered using filter paper and the filtrate was quenched with 51 mL of 0.1 N HCl (5.11 mmol). The layers were separated and the aqueous phase was extracted with 7 mL of dichloromethane. The combined organic phases were washed with water and then with brine, dried over Na2SO4, filtered, concentrated using a rotary evaporator, and dried in vacuo to give a crude pale yellow solid. The crude material was stirred with diethyl ether (50 mL) for 30 minutes, filtered on a glass frit, washed with diethyl ether, and dried in vacuo to give a pale yellow powder Boc-Gly-Rotigotine.HCl (1.258 g, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08597633B2
Source datasetuspto-grants-2013_12
ORD IDord-5ccfbe55755d4cbd92076028465e5564
Source noteuspto-grants-2013_12