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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889891Generated: November 1, 2026

Hydrochloric Acid → 7-Chlorothieno[3,2-b]pyridine-2-carbothioamide

https://huagongshe.com/reaction/889891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
Reactant7-Chloro-thieno[3,2-b]pyridine-2-carbothioic acid methoxymethyl amideHCID 85802105—
SolventTetrahydrofuranHCID 8028—
Product7-Chlorothieno[3,2-b]pyridine-2-carbothioamideHCID 2359510985%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-Chloro-thieno[3,2-b]pyridine-2-carbothioic acid methoxymethyl-amide (93.9 g, 344 mmol) and 900 mL THF was added 1 N HCl (344 mL, 344 mmol). The reaction mixture was heated to reflux for seventy-two hours. The reaction mixture was cooled to 0° C., and 300 mL of concentrated NH4OH was added and stirred. The THF was removed under reduced pressure and the residue was suspended in ethyl acetate and stirred. The precipitate was filtered, washed with ethyl acetate and dried to give 7-chloro-thieno[3,2-b]pyridine-2-carbothioic acid amide (66.7 g) in 85% yield. C8H5ClN2S2: APCI m/z: 228.9/230.9 (MH+); 1H NMR (d6-DMSO): δ 10.24 (s, 1H), 9.94 (s, 1H), 8.65 (d, 1H, J=5.0 Hz), 8.19 (s, 1H), 7.62 (d, 1H, J=5.0 Hz) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995171B2
Source datasetuspto-grants-2006_02
ORD IDord-09de6772c24f47988860595e7be7a232
Source noteuspto-grants-2006_02