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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829936Generated: October 31, 2026

4-Hydroxymethylpyridine → (1-{4-[3-Chloro-4-(pyridin-4-ylmethoxy)-phenylamino]-pyrrolo[2,1-f][1,2,4]triazin-5-ylmethyl}-piperidin-4-yl)-carbamic acid, tert-butyl ester

https://huagongshe.com/reaction/1829936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxymethylpyridineHCID 11472—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant{1-[4-(3-Chloro-4-hydroxy-phenylamino)-pyrrolo[2,1-f][1,2,4]triazin-5-ylmethyl]-piperidin-4-yl}-carbamic acid, tert-butyl esterHCID 21031521—
SolventTetrahydrofuranHCID 8028—
Product(1-{4-[3-Chloro-4-(pyridin-4-ylmethoxy)-phenylamino]-pyrrolo[2,1-f][1,2,4]triazin-5-ylmethyl}-piperidin-4-yl)-carbamic acid, tert-butyl esterHCID 21031526—

Reaction Steps

To a mixture of 21A (0.047 g, 0.1 mmol), triphenylphosphine (79 mg, 0.3 mmol), and 4-hydroxymethylpyridine (22 mg, 0.2 mmol) in dry THF was added diethyl azodicarboxylate (0.047 ml, 0.3 mmol). The mixture was stirred at room temperature overnight and purified by preparative HPLC to give Compound 21B as a colorless semi-solid (TFA salt). Analytical HPLC retention time=2.303 min. (Chromolith Speed ROD column 4.6×50 mm, 10–90% aqueous methanol over 4 minutes containing 0.2% trifluoroacetic acid, 4 mL/min, monitoring at 254 nm) and a LC/MS M++1=564+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064203B2
Source datasetuspto-grants-2006_06
ORD IDord-ae2ab1793b4945ae928e5cc8d4c1948c
Source noteuspto-grants-2006_06