Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575753Generated: October 30, 2026

Ammonia → 4-Bromo-6-methyl-7-oxothieno[2,3-c]pyridine-2-carboxamide

https://huagongshe.com/reaction/575753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 4-bromo-6-methyl-7-oxo-6,7-dihydrothieno[2,3-c]pyridine-2-carboxylateHCID 118021590—
SolventMethanolHCID 887—
Product4-Bromo-6-methyl-7-oxothieno[2,3-c]pyridine-2-carboxamideHCID 11802164595%

Reaction Conditions

Temperature45 °C

Reaction Steps

Using a sealed tube, a solution of methyl 4-bromo-6-methyl-7-oxothieno[2,3-c]pyridine-2-carboxylate (250 mg, 65 mmol) in MeOH (6 mL) stirred at rt was treated with 2N NH3 in methanol (8 ml). The sealed tube was heated to 45° C. for 60 h. After cooling to 0° C., the resulting suspension was filtered; the filter cake was washed with cooled (0° C.) MeOH (3 mL) and isopropyl ether (3 mL) to afford the title compound (215 mg, 95%) as a white solid. LCMS (M+H)+=288.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-e526f393bd7e4b58b3c8f33aef4ca7a4
Source noteuspto-grants-2015_05