HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877807Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 68155810, compound
https://huagongshe.com/reaction/1877807
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2,4,6-Trivinylboroxin-Pyridine Complex | HCID 2734806 | — |
| Reactant | HCID 68156188 | HCID 68156188 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Bis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+) | HCID 12976736 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68155810 | HCID 68155810 | — |
Reaction Steps
Mix methyl 3-[4-(2-bromo-7-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-yl)piperazin-1-yl]-2,2-dimethylpropanoate (1.00 equiv; 620.00 mg, 1.31 mmoles), triethenylboroxin pyridine (1.5 equiv; 472.79 mg, 1.96 mmoles;) in methanol (15 mL). Add a pre-blended mixture of 1.09 wt % tris(dibenzylideneacetonyl)bis-palladium (Pd2(dba)3), 1.16 wt % 1,1′-bis(di-tert-butylphosphino)ferrocene (dtbpf) and 97.75 wt % tripotassium phosphate (1.10 g) and heat at 140° C. for 25 mins in a microwave. Filter the reaction mixture through celite and dilute to 25 mL volume with methanol. Hydrogenate the methanolic solution by passing at 1 mL/min. through a H-Cube® flow hydrogenator using a 10% Pd/C catalytic cartridge at 50° C. Evaporate the solvent in vacuo to give methyl 3-[4-(2-ethyl-7-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-yl)piperazin-1-yl]-2,2-dimethylpropanoate. MS (m/z): 423.18 (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-d548251aa95c40eaa07caf0178dd75fd |
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| Source note | uspto-grants-2012_11 |
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