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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366785Generated: October 30, 2026

4-Methylmorpholine → HCID 23289903, compound

https://huagongshe.com/reaction/366785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Pyridineacetic acidHCID 34228—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant8-Chloro-5,11-dihydro-11-(1-piperazinyl)[1]benzothiepino[4,3-b]pyridineHCID 15780501—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 23289903HCID 2328990363%

Reaction Steps

DEC (464 mg, 2.42 mmol), HOBT (327 mg, 2.42 mmol), and 4-pyridine-acetic acid (332 mg, 2.42 mmol) were added to 1-(8-chloro-5,11-dihydro-[1]benzothiepino[4,3-b]pyridin-11-yl)-piperazine (400 mg, 1.21 mmol) and NMM (5.3 ml) in DMF (8 ml), and the mixture was stirred at room temperature for 19 hours. Water (30 ml) and EtOAc (50 ml) were added, and the layers were mixed and separated. The aqueous layer was extracted with EtOAc (3×40 ml). The aqueous layer was basified with saturated NaHCO3 and was extracted with CH2Cl2 (2×20 ml). The organic layers were combined, washed with brine, dried (Na2SO4), decanted and concentrated; the crude product (659 mg) was purified by flash chromatography (30%acetone/CH2Cl2 to 5%MeOH/CH2Cl2) and obtained as a white solid (344 mg, 63%); MS (FAB, M+H)=451; HRMS: calc.: 451.1359; found: 451.1355.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130229
Source datasetuspto-grants-2000_10
ORD IDord-b1e0f3326cd349119aa8c42037bf25e4
Source noteuspto-grants-2000_10