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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773614Generated: November 4, 2026

Sulfamic Acid → 2-Chlorothieno[3,2-D]pyrimidine-7-carboxylic acid

https://huagongshe.com/reaction/1773614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantSodium ChloriteHCID 23668197—
Reactant2-Chlorothieno[3,2-D]pyrimidine-7-carbaldehydeHCID 71741945—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Chlorothieno[3,2-D]pyrimidine-7-carboxylic acidHCID 5805630595.5%

Reaction Steps

To a suspension of 0.640 g (3.22 mmole) 2-chloro-thieno[3,2-d]pyrimidine-7-carbaldehyde in 20 mL of tetrahydrofuran, 10 mL of tert-butanol and 10 mL of water was added 1.25 g (12.9 mmole) of sulfamic acid. A solution of 0.729 g (8.06 mmole) sodium chlorite and 3.33 g (24.5 mmole) of potassium dihydrogen phosphate in 24 mL of water was slowly added via additional funnel. The reaction mixture was stirred at room temperature for over night. Water and ethyl acetate were added, separated. Aqueous layer was washed with ethyl acetate. Organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The solid residue was dried in high vacuum for over night to give 0.660 g of 2-chloro-thieno[3,2-d]pyrimidine-7-carboxylic acid as a yellow solid. MH+/Z=215

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-b5b0f64bfc14409abdac2d1ae3cba851
Source noteuspto-grants-2016_02