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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079620Generated: October 29, 2026

Triphenylphosphine → Tert-butyl 4-(7-bromo-2-chloroquinazolin-8-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2079620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant7-Bromo-2-chloroquinazolin-8-olHCID 59199227—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(7-bromo-2-chloroquinazolin-8-yloxy)piperidine-1-carboxylateHCID 5919924680%

Reaction Steps

A solution of DEAD (404 mg, 2.32 mmole) in THF (0.5 mL) was added to a solution of 7-bromo-2-chloroquinazolin-8-ol (400 mg, 1.54 mmole), tert-butyl 4-hydroxypiperidine-1-carboxylate (621 mg, 3.09 mmole) and PPh3 (610 mg, 2.32 mmole) in THF (5.5 mL) at RT. After 1.5 hours, silica gel was added to the reaction which was evaporated to dryness and loaded onto a flash column. The product was eluted with 25% EtOAc/hexane to give tert-butyl 4-(7-bromo-2-chloroquinazolin-8-yloxy)piperidine-1-carboxylate in 80% yield (545 mg, 1.23 mmole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932262B2
Source datasetuspto-grants-2011_04
ORD IDord-8756415a21a742d1bd0526ede76d7254
Source noteuspto-grants-2011_04