HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364016Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 66744039, compound
https://huagongshe.com/reaction/2364016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66744013 | HCID 66744013 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 66744039 | HCID 66744039 | 62% |
Reaction Steps
A mixture of 3-amino-5-bromo-N-(4-methoxybenzyl)thiophene-2-carboxamide (160 mg, 0.47 mmol), MgSO4 (60 mg), 2,2-dimethoxypropane (0.5 mL), PTSA (8.6 mg, 0.050 mmol) and DMA (0.5 mL) was stirred at 120° C. for 1 h by using microwave reactor. Then, the mixture was poured into saturated aqueous NaHCO3. The organic materials were extracted with AcOEt. The combined extracts were washed with water and brine, and then dried over Na2SO4. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (silica gel, 90:10 hexane/EtOAc to 40:60 hexane/EtOAc) to give the title compound (112 mg, 62%) as a pale brown solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691828B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2ffecb84bac647cd9ecfd63739755cc0 |
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| Source note | uspto-grants-2014_04 |
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