HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601303Generated: October 30, 2026
HCID 10314079, compound → HCID 136351968, compound
https://huagongshe.com/reaction/601303
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10314079 | HCID 10314079 | — |
| Reactant | 2-Amino-4-[(methoxymethoxy)methyl]-3-thiophenesulfonamide | HCID 57455187 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 136351968 | HCID 136351968 | 55.4% |
Reaction Steps
The product of Example 309G (110 mg, 0.43 mmol) and the product of Example 315B (140.6 mg, 0.43 mmol) were reacted in toluene (5 mL) at 100° C. for 3 hours. The reaction was concentrated under reduced pressure and the residue was purified by chromatography on silica gel using a Biotage-12 m column eluting with 1:99 methanol:dichloromethane to give the title compound as a white solid (114 mg, 54.6%). The sodium salt of the title compound was prepared according to the procedure of Example 1D. 1H NMR (300 MHz,CDCCl3) δ ppm 1.00 (t, J=7.35 Hz, 3 H), 1.46 (m, 2 H), 1.74 (m, 2 H), 3.45 (s, 3 H), 4.56 (m, 2 H), 4.80 (s, 2 H), 4.84 (s, 2 H), 7.09 (s, 1 H), 7.26 (s, 1 H), 7.36 (dd, J=8.09, 4.41 Hz, 1 H), 8.57 (dd, J=8.09, 1.84 Hz, 1 H), 8.81 (dd, J=4.78, 1.84 Hz, 1 H), 15.06 (s, 1 H), 15.11 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902203B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-4464ead5c7954194a94e10f6ebb47d29 |
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| Source note | uspto-grants-2011_03 |
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