HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877799Generated: November 3, 2026
Potassium Carbonate → HCID 68155976, compound
https://huagongshe.com/reaction/1877799
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2,2-dimethyl-3-(piperazin-1-yl)propanoate hydrochloride | HCID 68156003 | — |
| Reactant | HCID 68156097 | HCID 68156097 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68155976 | HCID 68155976 | 97.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314092B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-364366ad2ec347fbac059356986cf227 |
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| Source note | uspto-grants-2012_11 |
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