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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188011Generated: October 27, 2026

Pseudosaccharin chloride → HCID 178490771, compound

https://huagongshe.com/reaction/2188011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPseudosaccharin chlorideHCID 64783—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-7-aminomethyl-6-(4-methoxy-benzyl)-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid tert-butyl esterHCID 21936684—
SolventDichloromethaneHCID 6344—
ProductHCID 178490771HCID 17849077177.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-benzo[d]isothiazole-1,1-dioxide (160 mg, 0.79 mmol) and diisopropylethylamine (150 μl, 0.86 mmol) were dissolved in dichloromethane (7 ml) at 0° C. 2-Amino-7-aminomethyl-6-(4-methoxy-benzyl)-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid tert-butyl ester (284 mg, 0.70 mmol) was added and the mixture was stirred for 15 minutes at 0° C., diluted with dichloromethane (10 ml) and washed with water (20 ml) and brine (20 ml). The organic phase was dried (MgSO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a gradient of hexanes/ethyl acetate (1:1) to pure ethyl acetate as eluent, which afforded 309 mg (77%) of 2-amino-7-((1,1-dioxo-1H-benzo[d]isothiazol-3-ylamino)methyl)-6-(4-methoxy-benzyl)-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid tert-butyl ester as an foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410556B1
Source datasetuspto-grants-2002_06
ORD IDord-db0176a047c5463fb17bacc999b74f79
Source noteuspto-grants-2002_06