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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877799Generated: November 3, 2026

Potassium Carbonate → HCID 68155976, compound

https://huagongshe.com/reaction/1877799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2,2-dimethyl-3-(piperazin-1-yl)propanoate hydrochlorideHCID 68156003—
ReactantHCID 68156097HCID 68156097—
SolventAcetonitrileHCID 6342—
ProductHCID 68155976HCID 6815597697.4%

Reaction Steps

To a suspension of 7,11-dichloro-2-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepine (34.0 g, 128.23 mmoles) in acetonitrile (300 mL) add methyl 2,2-dimethyl-3-(piperazin-1-yl)-propionate hydrochloride (2.1 equiv; 63.75 g, 269.29 mmoles) and potassium carbonate (4 equiv; 70.89 g, 512.93 mmoles). Heat the mixture at reflux overnight. Evaporate to dryness. Partition the residue between water (500 mL) and EtOAc (2×500 mL). Combine the organic layers and wash with water (500 mL) then brine. Dry over sodium sulfate, filter and evaporate to a brown oil. Add iso-hexane (˜150 mL) and a seed crystal of Preparation 50. Allow to crystallize over 2 h, then transfer the flask to a fridge and allow to stand. Collect the resulting heavy crystalline solid by filtration, washing with cold iso-hexane. Dry in a vacuum oven at 40° C. for 1 h, to give methyl 3-[4-(7-chloro-2-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-yl)piperazin-1-yl]-2,2-dimethylpropanoate (53.6 g, 97% yield). MS (m/z): 429.18 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314092B2
Source datasetuspto-grants-2012_11
ORD IDord-364366ad2ec347fbac059356986cf227
Source noteuspto-grants-2012_11