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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951192Generated: October 26, 2026

(4-Methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amine → 4-Methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-ylamine

https://huagongshe.com/reaction/1951192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amineHCID 86610335—
SolventTrifluoroacetic acid waterHCID 22392675—
Product4-Methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-ylamineHCID 86610336—

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution comprising (4-methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amine (25c) (0.45 g, 1.13 mmol) in trifluoroacetic acid:water (95:5) (10 ml) is heated at 75° C. for days. The solvent is removed in vacuo and the crude residue is dissolved in ethyl acetate. The pH is adjusted to pH12 using 2N sodium hydroxide and the layers are separated. The aqueous layer is extracted with ethyl acetate (2×30 ml). The organic portions are combined and washed with brine (50 ml), dried over MgSO4 and concentrated in vacuo to yield the titled compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404684B2
Source datasetuspto-grants-2013_03
ORD IDord-8c7f8a191e05474a866482fb25528157
Source noteuspto-grants-2013_03