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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723234Generated: November 1, 2026

HCID 145857648, compound → HCID 21886278, compound

https://huagongshe.com/reaction/723234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 145857648HCID 145857648—
CatalystTrifluoroacetic acidHCID 6422—
SolventDichloromethaneHCID 6344—
ProductHCID 21886278HCID 2188627894.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-methylsulfanyl-4-(3-piperidin-1-yl-benzenesulfonyl)-thiophene-2-carboxamidine (10 mg, 0.020 mmol, Example 286: step h) in 1 mL of CH2Cl2 under Ar at 0° C. was added 5 drops (˜200 ul) of TFA. The mixture was stirred at 0° C. for 1 h. Removal of the solvent under reduced pressure followed by flash chromatography of the residue on silica gel (5% MeOH/CH2Cl2) gave 7.5 mg (77%) of product as colorless oil: 1H-NMR (CD3OD, 400 MHz) δ 8.25 (s, 1H), 7.76 (dd, 1H, J=1.6, 1.6 Hz), 7.62 (ddd, 1H, J=7.5, 1.6, 1.6 Hz), 7.56 (ddd, 1H, J=7.5, 1.6, 1.6 Hz), 7.51 (dd, 1H, J=7.5, 7.5), 3.31–3.30 (m, 4H), 2.54 (s, 3H), 1.57–1.56 (m, 6H). Mass spectrum (ESI, m/z): Calcd. for C17H21N3O2S3, 396.1 (M+H), found 396.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-f572ee11367142cdac2e5fcb9b8f1237
Source noteuspto-grants-2006_11