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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108350Generated: October 31, 2026

Dimethylformamide → 4,5-Dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxamide

https://huagongshe.com/reaction/1108350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant4,5-Dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxylic acidHCID 12043506—
SolventTetrahydrofuranHCID 8028—
Product4,5-Dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxamideHCID 1204351057%

Reaction Steps

4,5-Dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxylic acid (0.47 g) was suspended in tetrahydrofuran (15 ml); oxalyl chloride (0.32 g) and then N,N-dimethylformamide (6 μl) were added. After this mixture was stirred at room temperature for 2 hours, it was concentrated under reduced pressure. The residue was suspended in tetrahydrofuran (5 ml) and cooled with ice; concentrated aqueous ammonia (4.0 ml) was added. After the reaction mixture was stirred at room temperature for 1 hour, it was poured over water (150 ml) and extracted with ethyl acetate-tetrahydrofuran (3:1, v/v). The organic layer was washed with water and dried (MgSO4), after which the solvent was distilled off to yield 4,5-dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxamide (0.27 g, 57%), which was then recrystallized from chloroform-methanol. Light-yellow needles. Melting point over 300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066658
Source datasetuspto-grants-2000_05
ORD IDord-e57ab7bfcc7843a7989d4594a9bfddce
Source noteuspto-grants-2000_05