HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591737Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 136348020, compound
https://huagongshe.com/reaction/591737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Amino-4,6-dimethoxybenzamide | HCID 20349016 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 61669147 | HCID 61669147 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 136348020 | HCID 136348020 | — |
Reaction Steps
To a solution of 2-amino-4,6-dimethoxy-benzamide (1.3 g, 6.63 mmol) and 4-(3-hydroxypropoxy)-3,5-dimethyl benzaldehyde (1.38 g, 6.63 mmol) in N,N-dimethyl acetamide (10 mL), NaHSO3 (1.30 g, 7.3 mmol), and p-TSA (252 mg, 1.32 mmol) were added and the reaction mixture was heated at 115° C. for 26 hours, then cooled to room temperature. The solvent was removed under reduced pressure. Then, water (100 mL) was added and stirred for 1 hour at room temperature. The separated solids were filtered and dried. The solids were again washed with diethyl ether to give crude product 2-[4-(3-hydroxy-propoxy)-3,5-dimethyl-phenyl]-5,7-dimethoxy-3H-quinazolin-4-one as an off-white solid. Yield: 1.69 g (66%).
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-d6a3ca2e175b4988b46fc37230ed9e50 |
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| Source note | uspto-grants-2016_01 |
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