HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591690Generated: October 31, 2026
p-Toluenesulfonic acid monohydrate → HCID 178493403, compound
https://huagongshe.com/reaction/591690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-Amino-4,6-dimethoxybenzamide | HCID 20349016 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 178519378 | HCID 178519378 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178493403 | HCID 178493403 | — |
Reaction Steps
To a solution of 3-(tetrahydro-pyran-2-yloxymethyl)-1H-indazole-5-carbaldehyde (0.32 g, 1.23 mmol) and 2-amino-4,6-dimethoxy-benzamide (0.24 g, 1.23 mmol) in N,N-dimethylacetamide (10 mL) were added NaHSO3 (58.5 wt %, 0.27 g, 1.48 mmol) and p-toluenesulfonic acid monohydrate (0.05 g, 0.25 mmol); the reaction mixture was heated at 120° C. for 16 hours, then cooled to room temperature. Solvent was removed under reduced pressure. The residue was diluted with water (100 mL). The separated solid was filtered and washed with water and dried under vacuum. The residue was purified by the Simpliflash system (0-5% methanol in CH2Cl2 as eluent) to give the title compound as an off-white solid. Yield: 30 mg (7%). MP 264-266° C. 1H NMR (400 MHz, CD3OD): δ 8.60 (s, 1H), 8.10 (d, J=8.98 Hz, 1H), 7.65 (d, J=8.98 Hz, 1H), 6.85 (d, J=1.95 Hz, 1H), 6.55 (d, J=1.95 Hz, 1H), 5.05 (s, 2H), 3.96 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238640B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-097decc652d742dd894d9471e19c043d |
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| Source note | uspto-grants-2016_01 |
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