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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385086Generated: October 30, 2026

Formaldehyde → 3-(3,5-Difluoro-4-methoxybenzoyl)-2,3-dihydro-1,3-benzothiazole

https://huagongshe.com/reaction/385086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzothiazolineHCID 96588—
Reactant3,5-Difluoro-4-methoxybenzoyl chlorideHCID 17750662—
SolventDichloromethaneHCID 6344—
Product3-(3,5-Difluoro-4-methoxybenzoyl)-2,3-dihydro-1,3-benzothiazoleHCID 68109091—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (316 mg) and 37% formalin (0.21 mL) in the same manner as in Example 1 was dissolved in dichloromethane (3 mL), and diisopropylethylamine (0.56 mL) and 3,5-difluoro-4-methoxybenzoyl chloride (347 mg) were added to the solution, and then the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was used for the synthesis of (c).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-a27f23469c86497395b4ff7e7ae02db8
Source noteuspto-grants-2013_02