HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979496Generated: October 31, 2026
N,N-Dimethyl-1,3-propanediamine → HCID 13646117, compound
https://huagongshe.com/reaction/979496
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | HCID 13646085 | HCID 13646085 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 13646117 | HCID 13646117 | 42% |
Reaction Steps
2.84 g (8 mmol) of 2-(2,5-dimethoxyphenylmethyl)-6-isopropoxy-4H-3,1-benzoxazin-4-one and 0.82 g (8 mmol) of 3-dimethylaminopropylamine were heated under reflux for 15 hours in xylene (20 ml). After the xylene was distilled off, the residue obtained was purified by silica gel column chromatography (eluent; 2% ethanol/chloroform) to obtain 1.46 g (42%) of 2-(2,5-dimethoxyphenylmethyl)-3-(3-dimethylaminopropyl)-6-isopropoxy-4(3H)-quinazolinone as an oily substance. Subsequently, 0.22 g of the 2-(2,5-dimethoxyphenylmethyl)-3-(3-dimethylaminopropyl)-6-isopropoxy-4(3H)-quinazolnone was dissolved in ether (15 ml) and to the resulting soluion, there was added an ethanolic solution containing 0.07 g (0.6 mmol) of maleic acid. The thus obtained solution was allowed to stand for one day. The precipitated colorless crystals were collected by filtration to obtain 0.25 g of the maleate which is the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668682 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-9699f208bcdf41539bf7260ecf957300 |
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| Source note | uspto-grants-1987_05 |
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