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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980225Generated: October 30, 2026

Hydrochloric Acid → HCID 13578786, compound

https://huagongshe.com/reaction/980225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-AcetamidothiazoleHCID 17625—
ReactantHCID 13578774HCID 13578774—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 13578786HCID 1357878652.8%

Reaction Conditions

Temperature-75 °C

Reaction Steps

A solution of 85.6 ml of n-butyllithium in hexane was introduced into 8.5 g of N-2-thiazolyl acetamide suspended in 260 ml of tetrahydrofuran. After cooling to -75° C., a solution of 10.33 g of the product of Step A in 75 ml of tetrahydrofuran was added at this temperature. The reaction mixture was poured into 400 ml of water and 100 ml of 2N hydrochloric acid, and was extracted with ether. The organic phase was washed with N hydrochloric acid, then with water, dried, and concentrated to dryness under reduced pressure. The orange oil residue crystallized and the residue was triturated in ether, separated, washed with ether, and dried under reduced pressure to obtain 7.7 g of 1,1-dimethylethyl N-[2-[[2-[1,3-dioxo-3-(2-thiazolylamino)-propyl]-6-trifluoromethylphenyl]-amino]-2-oxo-ethyl]-carbamate melting at 166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636512
Source datasetuspto-grants-1987_01
ORD IDord-af07b7d8456045caabff3132a407e26c
Source noteuspto-grants-1987_01