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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729721Generated: October 29, 2026

Acetonitrile → HCID 21093936, compound

https://huagongshe.com/reaction/729721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 21094164HCID 21094164—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 21093936HCID 21093936—

Reaction Conditions

Temperature20 °C

Reaction Steps

Ethyl 2-aminothiazole-5-carboxylate (2.21 g, 12.8 mmol) was condensed with 2-(4-methanesulfonylphenyl)-3-(tetrahydropyran-4-yl)propionic acid (Preparation 41, 1.00 g, 3.2 mmol) using the procedure described for EXAMPLE 65, to give ethyl 2-[2-(4-methanesulfonylphenyl)-3-(tetrahydropyran-4-yl)propionylamino]thiazole-5-carboxylate: m/z (ES+)=508.3 [M+MeCN+H]+. LiOH.H2O (410 mg, 9.8 mmol) was added to a solution of this ester (1.44 g, 3.1 mmol) in THF-H2O (3:1, 30 mL). The mixture was stirred at 20° C. for 16 h and then at 55° C. for 24 h. The solvents were removed in vacuo, then the residue was dissolved in H2O (50 mL). The aqueous solution was washed with EtOAc (20 mL), before being acidified to pH 1 with 2M HCl and extracted with EtOAc (2×100 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated to give a solid that was recrystallised (EtOAc-MeOH) to give the title compound: RTA=29.5 min; m/z (ES+)=480.2 [M+MeCH+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582632B2
Source datasetuspto-grants-2009_09
ORD IDord-fe036d7c82d644e4b71f590f871b8047
Source noteuspto-grants-2009_09