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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440774Generated: October 29, 2026

2-(Tributylstannyl)pyridine → 10,11-Dihydro-10-[4-(2-pyridinyl)benzoyl]-5H-pyrrolo[2,1-c][1,4]benzodiazepine

https://huagongshe.com/reaction/440774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)pyridineHCID 607784—
ReactantHCID 15298021HCID 15298021—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product10,11-Dihydro-10-[4-(2-pyridinyl)benzoyl]-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 2240533081.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2.0 g of 10,11-dihydro-10-(4-iodobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine and 4.39 g of 2-[(tri-n-butyl)stannyl]pyridine in 30 ml of toluene under nitrogen is added 0.2 g of tetrakis(triphenylphosphine)palladium and the mixture heated to 120° C. for 16 hours. The toluene is evaporated in vacuo and the oily residue diluted with 50 ml of chloroform and washed with water, dried (Na2SO4), filtered through diatomaceous earth and evaporated in vacuo to give a residue which is columned on silica gel by elution with 7:1 to 1:1 ethyl acetate:hexane to give 1.44 g of the desired product as a solid, m.p. 170°-172° C.; M+H=366.1; M+Na=388.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521173
Source datasetuspto-grants-1996_05
ORD IDord-0af347db7cd14409b399f7dbd23d2965
Source noteuspto-grants-1996_05