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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908034Generated: October 30, 2026

Hydrochloric Acid → HCID 58551479, compound

https://huagongshe.com/reaction/1908034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
ReactantLawesson's reagentHCID 87949—
ReactantHCID 58551093HCID 58551093—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58551479HCID 5855147999.1%

Reaction Steps

tert-Butyl 3-amino-4-oxo-spiro[chromane-2,4′-piperidine]-1′-carboxylate (33 mg, 0.10 mmol), acetyl chloride (7.8 μL, 0.11 mmol), and N,N-diethylethanamine (28 μL, 0.20 mmol) were combined in dichloromethane and stirred for 30 minutes. The reaction mixture was diluted with dichloromethane and was washed with 1N HCl, a saturated solution of NaHCO3, and brine. The organics were dried over sodium sulfate and evaporated to dryness. The residue was stirred in toluene with Lawesson's reagent (40 mg, 0.10 mmol) at 70° C. overnight. The reaction was diluted with dichloromethane and filtered through a pad of Celite. The filtrate was evaporated and stirred with HCl in dioxane (1.0 mL of 4.0 M, 4.0 mmol) for 1 h at room temperature. The reaction mixture was evaporated to dryness to yield 2-methylspiro[chromeno[3,4-d]thiazole-4,4′-piperidine] (27 mg, 20%). ESI-MS m/z calc. 272.4. found 273.1 (M+1)+; Retention time: 1.05 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-b634b73546c44fc8b190801716a7fbe8
Source noteuspto-grants-2013_12