HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548745Generated: October 29, 2026
Potassium Carbonate → HCID 57663179, compound
https://huagongshe.com/reaction/548745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-fluoro-2-methyl-3,4-dihydro-2H-5,1,2-benzoxathiazepine 1,1-dioxide | HCID 57663178 | — |
| Reactant | 3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoic acid | HCID 57663224 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57663179 | HCID 57663179 | 57.1% |
Reaction Steps
A mixture of 3-hydroxy-5-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}benzoic acid (0.2 g, 0.88 mmol), 7-fluoro-2-methyl-3,4-dihydro-2H-5,1,2-benzoxathiazepine 1,1-dioxide (205 mg, 0.88 mmol) and potassium carbonate (244 mg, 1.77 mmol) in acetonitrile (5 mL) was stirred in a microwave reactor at 120° C. for 28 hours. The solvent was removed in vacuo and water (50 mL) and ethyl acetate (50 mL) added. The ethyl acetate layer was separated and discarded and the aqueous layer acidified and extracted into ethyl acetate (2×50 mL). The combined organics were washed with brine, dried (MgSO4), filtered and the solvent removed in vacuo to give the desired compound as a brown oil (0.22 g) which was used in the following steps without further purification. m/z 436 (M−H)−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943607B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-b58a653b70e543918e062ee57ae81ed5 |
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| Source note | uspto-grants-2011_05 |
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