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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212877Generated: October 31, 2026

Tetrahydrofuran → HCID 21955962, compound

https://huagongshe.com/reaction/2212877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 21955967HCID 21955967—
ReactantHCID 178418332HCID 178418332—
ProductHCID 21955962HCID 21955962—

Reaction Steps

To a suspension of N-[4-(2-amino-4-phenyl-thiazol-5-yl)-pyrimidin-2-yl]-N-(3-methoxycarbonyl-phenyl)-amine (800 mg, 2.0 mmol) in tetrahydrofuran (30 ml) is added a solution of methyl magnesium chloride (6 ml of a 20% THF solution) without cooling. The temperature of the reaction mixture rises to about +45° C. and the starting material dissolves immediately yielding a yellow clear solution. After an additional hour the solution is poured onto crushed ice and ammonium chloride. The colorless precipitate is filtered and washed with ethyl acetate and tetrahydrofuran. The organic phases are pooled, dried and concentrated under reduced pressure. Chromatography of the resulting solid gives the N-[4-(2-amino-4-phenyl-thiazol-5-yl)-pyrimidin-2-yl]-N-[3-(2-hydroxy-2-methyl-ethyl)-phenyl]-amine, m.p. 219–220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105517B2
Source datasetuspto-grants-2006_09
ORD IDord-5d7e34af201e46a69f09c1d45516fbab
Source noteuspto-grants-2006_09