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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670572Generated: November 3, 2026

Succinic Acid → 6-(5-Amino-[1,2,4]thiadiazol-3-ylthiomethyl)-7-chloro-2,3,4,5-tetrahydro-1H-benzo[d]azepine Succinate

https://huagongshe.com/reaction/1670572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic AcidHCID 1110—
Reactant6-(5-amino-[1,2,4]thiadiazol-3-ylthiomethyl)-7-chloro-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 59822304—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product6-(5-Amino-[1,2,4]thiadiazol-3-ylthiomethyl)-7-chloro-2,3,4,5-tetrahydro-1H-benzo[d]azepine SuccinateHCID 67336313100%

Reaction Steps

Add succinic acid (0.035 g, 0.299 mmol) to a mixture of 6-(5-amino-[1,2,4]thiadiazol-3-ylthiomethyl)-7-chloro-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.098 g, 0.299 mmol) in absolute ethanol (5 mL), DCM (5 mL) and methanol (2 mL) at room temperature. Concentrate the reaction mixture in vacuo. Combine the residue with methanol (5 mL) and DCM (5 mL) and concentrate in vacuo. Combine the residue with MTBE (5 mL) and concentrate three times to afford a white solid. Dry under high vacuum at room temperature overnight to afford the title compound (0.133 g, 100%) as a white solid. MS (ES+) m/z: 327.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994163B2
Source datasetuspto-grants-2011_08
ORD IDord-b6d016e0d83e443d92b557d8353e09fd
Source noteuspto-grants-2011_08