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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455680Generated: November 1, 2026

Triphenylphosphine → tert-Butyl 4-(4-{[(5-chloro-2-thienyl)carbonyl]amino}-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)tetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/1455680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant5-Chloro-N-(1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl)thiophene-2-carboxamideHCID 4135740—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(4-{[(5-chloro-2-thienyl)carbonyl]amino}-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)tetrahydro-1(2H)-pyridinecarboxylateHCID 18440735—

Reaction Steps

At room temperature, 0.12 ml (0.76 mmol) of diethyl azodicarboxylate (DEAD) is added dropwise to a suspension of 150 mg (0.49 mmol) of 5-chloro-N-(1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl)-2-thiophenecarboxamide, 148 mg (0.73 mmol) of tert-butyl 4-hydroxytetrahydro-1(2H)-pyridinecarboxylate and 199 mg (0.76 mmol) of triphenylphosphine in 1.95 ml of absolute THF. After 2 h at room temperature, the mixture is concentrated and the residue is separated by chromatography on silica gel (dichloromethane/methanol mixture) and the product is isolated. Yield: 184 mg (76.8% of theory); MS (LC-MS): m/z (%)=279 (M+H, 100); LC-MS (Method 4): rt (%)=3.88 (98.9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482472B2
Source datasetuspto-grants-2009_01
ORD IDord-b19c7f0a7e4c4d519a83bb96e40100d7
Source noteuspto-grants-2009_01