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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604891Generated: October 30, 2026

Water → HCID 86624686, compound

https://huagongshe.com/reaction/604891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
ReactantHeptaneHCID 8900—
ReactantHCID 86624685HCID 86624685—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86624686HCID 8662468699%

Reaction Steps

To a solution of 80 mg (0.94 mmol) piperidine in dioxane (1 ml) 2M trimethylaluminium solution in heptane (0.94 mmol, 0.47 ml) was carefully added. The solution was stirred at room temperature for 1 hour. A suspension of 100 mg (0.27 mmol) ({2-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-thiazol-4-yl}-acetic acid ethyl ester in dioxane (3 ml) was added and the reaction was refluxed over night. Water was added carefully and the reaction was extracted twice with ethyl acetate. The organic layer was dried over sodium sulphate, filtered and the solvent was evaporated under reduced pressure to yield 110 mg (99%) 2-{2-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-thiazol-4-yl}-1-piperidin-1-yl-ethanone as a brown foam. MS ISP (m/e): 410.1 (100) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.35 (s, 1H), 7.70 (s, 1H), 7.65 (s, 1H), 7.23 (d, 1H), 7.17 (d, 1H), 7.03 (s, 1H), 6.64 (s, 1H), 3.79 (s, 3H), 3.67 (s, 2H), 3.49 (br t, 2H), 3.42 (br t, 2H), 2.14 (s, 3H), 1.58-1.32 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910740B2
Source datasetuspto-grants-2011_03
ORD IDord-e722721842424828b2213bd755d2bb72
Source noteuspto-grants-2011_03