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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30154Generated: October 25, 2026

Cyanamide → HCID 11951440, compound

https://huagongshe.com/reaction/30154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
Reactant3-Fluorophenacyl bromideHCID 2737451—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantTert-butyl 4-isothiocyanatopiperidine-1-carboxylateHCID 58591952—
SolventAcetonitrileHCID 6342—
Solventtert-ButanolHCID 6386—
ProductHCID 11951440HCID 1195144062%

Reaction Steps

At 20° C., a mixture of 4-isothiocyanatopiperidine-1-carboxylic acid tert-butyl ester (2.4 g, 10 mmol) (Example 1) and cyanamide (0.42 g, 10 mmol) (Aldrich) in tert-butanol (5 mL) and acetonitrile (35 mL) was treated with potassium tert-butoxide (1.0 M/THF, 10 mL, 10 mmol, Aldrich) for 15 min. 2-bromo-1-(3-fluorophenyl)ethanone (2.0 g, 9.2 mmol)(Example 2) was added and the suspension was stirred for 2 h. Solvent was removed and the solid residue purified by silica gel chromatography (60%-70% ethyl acetate/hexane) to give 2.4 g (57% yield) of 4-[4-amino-5-(3-fluorobenzoyl)thiazol-2-ylamino]piperidine-1-carboxylic acid tert-butyl ester. 1H NMR (DMSOd6, 300 MHz) δ1.36 (m, 2H, NCH2), 1.41 (s, 9H, 3CH3), 1.88 (m, 2H, NCH2), 2.88 (brd, 2H, NCH2), 3.6-4.0 (m, 1H, CH), 3.87 (m, 2H, NCH2), 7.31 (t, 1H, Aromatic), 7.38 (d, 1H, Aromatic), 7.48 (t, 1H, Aromatic), 7.51 (q, 1H, Aromatic), 8.01 (brd, 1H, NH), 8.48 (brd, 1H, NH), 8.48 (brd, 1H, NH), 8.70 (brd, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423053B2
Source datasetuspto-grants-2008_09
ORD IDord-5e57653588dc43ecb5e27ecefe2851a2
Source noteuspto-grants-2008_09