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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715281Generated: November 1, 2026

Triethylamine → HCID 11989990, compound

https://huagongshe.com/reaction/1715281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperazin-2-oneHCID 231360—
ReactantHCID 86621993HCID 86621993—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11989990HCID 1198999025%

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). Piperazin-2-one (Aldrich) (63.7 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 (41) as a yellow powder (47.7 mg; 25%). 1H NMR (DMSO-d6, 300 MHz) δ 2.14 (s, 3H), 2.48 (s, 3H), 3.25-3.40 (m, 2H), 3.82 (m, 1H), 4.15 (m, 1H), 4.45 (m, 1H), 4.86 (m, 1H), 8.03 (s, 1H), 8.19 (br s, 1H), 12.17 (s, 1H). M− (ESI): 364.05; M+ (ESI): 365.97. HPLC (method A), Rt: 2.14 min (purity: 99.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799814B2
Source datasetuspto-grants-2010_09
ORD IDord-ed96cb89a6a3445ab263ba380dfa3a96
Source noteuspto-grants-2010_09