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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877807Generated: November 1, 2026

Potassium Phosphate, Tribasic → HCID 68155810, compound

https://huagongshe.com/reaction/1877807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
ReactantHCID 68156188HCID 68156188—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystBis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+)HCID 12976736—
SolventMethanolHCID 887—
ProductHCID 68155810HCID 68155810—

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314092B2
Source datasetuspto-grants-2012_11
ORD IDord-d548251aa95c40eaa07caf0178dd75fd
Source noteuspto-grants-2012_11