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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063515Generated: November 1, 2026

Formic Acid → 2-(2,6-Dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/2063515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantEthanolHCID 702—
ReactantThioureaHCID 2723790—
ReactantHCID 57742481HCID 57742481—
Product2-(2,6-Dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidineHCID 6851917041%
ProductHCID 178503525HCID 17850352518%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of N-(4,6-dichloro-2-methylsulfanyl-pyrimidin-5-yl)-2-(2,6-dichloro-phenyl)-acetamide (10 g, 25 mmol), thiourea (1.9 g, 25 mmol), and EtOH (100 mL) was added formic acid (0.8 mL) at rt. The resulting mixture was heated to 90° C. After 12 h, the reaction mixture was cooled and concentrated. The resulting residue was collected by vacuum filtration and washed with H2O (50 mL) followed by hexanes (50 mL). The title compound purified by FCC to afford 2-(2,6-dichloro-benzyl)-5-methylsulfanyl-thiazolo[5,4-d]pyrimidin-7-ol (1.6 g, 18%) and 2-(2,6-dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine (4 g, 41%) as colorless solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288397B2
Source datasetuspto-grants-2012_10
ORD IDord-65a3cdb675ba47b286d6a3afb001b565
Source noteuspto-grants-2012_10