HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromaleic anhydride → HCID 86740704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromaleic anhydride | HCID 70728 | — |
| Reactant | HCID 54343992 | HCID 54343992 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86740704 | HCID 86740704 | 31.7% |
Reaction Steps
6-amino-3-benzylidene-1,2,3,9-tetrahydro-pyrrolo[2,1-b]quinazoline-9-one (2 g) was reacted with 2,3-dichloro-maleic anhydride (3.46 g) in tetrahydrofuran (130 ml) under stirring at the reflux temperature for 3 hours. After cooling the solution was evaporated in vacuo to dryness: the residue was suspended in hot ethyl acetate and filtered. Crystallization from CH2Cl2 -ethyl acetate gave 1 g of (Z)-3-[N-(3-benzylidene-9-oxo-1,2,3,9-tetrahydro-pyrrolo[2,1-b]quinazolin-6-yl)-aminocarbonyl]-2,3-dichloro-2-propenoic acid, m.p. 160°-165° C. (dec.),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04579847 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-172b758317174b9f9afc6d5124f52d62 |
| Source note | uspto-grants-1986_04 |