HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717361Generated: November 1, 2026
3,4,5-Trimethoxybenzaldehyde → HCID 178486783, compound
https://huagongshe.com/reaction/717361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 2-Amino-4,5-dimethoxybenzamide | HCID 10867236 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178486783 | HCID 178486783 | — |
Reaction Steps
Into a 500-mL 3-necked round-bottom flask, was placed 2-amino-4,5-dimethoxybenzamide (12 g, 61.16 mmol, 1.00 equiv), dimethylacetamide (200 mL), 3,4,5-trimethoxybenzaldehyde (12 g, 61.16 mmol, 1.00 equiv) and NaHSO3 (9.55 g, 91.83 mmol, 1.50 equiv). The resulting solution was stirred overnight at 139° C. The mixture was cooled to room temperature. The resulting solution was diluted with 800 mL of water. The solids were collected by filtration. The filter cake was washed with 1×100 ml of water, 100 ml of diethyl ether and 100 mL of methanol. This resulted in 12 g (53%) of 6,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)quinazolin-4-ol as a brown solid. MS (ESI) m/z 373 [M+h]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193707B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-c99429e3cc334846961346b74a8360c6 |
|---|
| Source note | uspto-grants-2015_11 |
|---|