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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175657Generated: October 29, 2026

Tricyclohexylphosphine → HCID 86719395, compound

https://huagongshe.com/reaction/2175657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclohexylphosphineHCID 75806—
ReactantMethylboronic AcidHCID 139377—
ReactantHCID 86719393HCID 86719393—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 86719395HCID 8671939561%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of (R)-tert-butyl 3-(4-amino-6-bromo-5-(4-((1-(pivaloyloxymethyl)-1H-1,2,3-triazol-5-yl)methoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate (82) (344 mg, 0.51 mmol) in toluene (10 mL) were added methylboronic acid (306 mg, 5.1 mmol), Pd2(dba)3 (23.3 mg, 0.0255 mmol), PCy3 (14.3 mg, 0.051 mmol) and K3PO4.3H2O (407 mg, 1.53 mmol). The resulting mixture was purged with N2 for three times before heated to 120° C. overnight. The solvents were removed under vacuum and the residue was purified by flash chromatography (silica gel, 0 to 15% MeOH in DCM, with 0.5% TEA) to provide (R)-tert-butyl 3-(4-amino-6-methyl-5-(4-((1-(pivaloyloxymethyl)-1H-1,2,3-triazol-5-yl)methoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate (83) (188 mg, 61%). LC-MS (ESI): m/z (M+1) 605.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062058B2
Source datasetuspto-grants-2015_06
ORD IDord-b46952dd78fb486685cac2c9d78b9e9c
Source noteuspto-grants-2015_06