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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82148Generated: October 27, 2026

7-(2-{[tert-butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine → [7-(2-{[tert-Butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]{5-[(diphenylmethylene)amino]pyridin-3-yl}methanone

https://huagongshe.com/reaction/82148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(2-{[tert-butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidineHCID 70817672—
Reactant5-((Diphenylmethylene)amino)-N-methoxy-N-methylnicotinamideHCID 86672080—
Product[7-(2-{[tert-Butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]{5-[(diphenylmethylene)amino]pyridin-3-yl}methanoneHCID 86672081—

Reaction Steps

The title compound was prepared according to the method described for Preparation 24 using 7-(2-{[tert-butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine (see Preparation 15) and 5-[(diphenylmethylene)amino]-N-methoxy-N-methylnicotinamide (see Preparation 23) to afford the title compound as a colourless gum in 56% yield, 1.49 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-19ba1702d8234d8bb5f6bce3230c1d2c
Source noteuspto-grants-2014_09