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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715282Generated: November 2, 2026

Triethylamine → HCID 11990104, compound

https://huagongshe.com/reaction/1715282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperonylamineHCID 2723901—
ReactantHCID 86621993HCID 86621993—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11990104HCID 1199010420%

Reaction Steps

2′-Acetylamino-4′-methyl-[4,5′]bithiazolyl-2-carbonyl chloride, prepared as in Step I of Example 13, described above (160 mg; 0.53 mmol; 1 eq.), is dissolved in THF (8 ml) and DCM (4 ml). 4-Piperidone hydrochloride monohydrate (Aldrich) (97.7 mg; 0.64 mmol; 1.20 eq.) and triethylamine (0.22 ml; 1.59 mmol; 3 eq.) are added and the mixture is stirred overnight at rt. Solvents are evaporated and the crude product is purified by preparative HPLC, affording Compound (42) as a pale yellow powder (39.2 mg; 20%). 1H NMR (DMSO-d6, 300 MHz) δ 2.14 (s, 3H), 2.49 (s, 3H), 2.53 (m, 4H), 3.94 (m, 2H), 4.53 (m, 2H), 8.03 (s, 1H), 12.17 (s, 1H). M− (ESI): 363.09; M+ (ESI): 365.04. HPLC (method A), Rt: 2.44 min (purity: 95.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799814B2
Source datasetuspto-grants-2010_09
ORD IDord-978dad0c1bb84e669b8444e11fd70186
Source noteuspto-grants-2010_09