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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795018Generated: October 26, 2026

Ytterbium → tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylate

https://huagongshe.com/reaction/1795018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantYtterbiumHCID 23992—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazoleHCID 21023606—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylateHCID 29943209—

Reaction Steps

To a solution of 5-[((2R)oxiran-2-yl)methoxy]-2-methylbenzothiazole, a compound of formula (3) (6.2 g, 28 mmol), and tert-butyl 1-piperazinecarboxylate, a compound of formula (4) (5.7 g, 31 mmol), in methylene chloride (200 ml), was added ytterbium (111) trifluoromethanesulfonate (1.73 g, 28 mmol). The resulting solution was allowed to stir at room temperature overnight. The solvent was evaporated (in vacuo), to yield a semi-solid, which was chromatographed on silica gel, eluting with 5% methanol/methylene chloride, to yield tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylate as a clear oil (9.5 g, 23 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026321B2
Source datasetuspto-grants-2006_04
ORD IDord-2d2f5e3f785343e0bc417fa9378ae1b8
Source noteuspto-grants-2006_04