HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Amino-6-[(1-methoxy-2-methylindolizin-3yl)carbonyl]quinazoline-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate | HCID 66653263 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Amino-6-[(1-methoxy-2-methylindolizin-3yl)carbonyl]quinazoline-2,4(1H,3H)-dione | HCID 66653327 | 10.7% |
Reaction Steps
0.123 g (0.41 mmol) of triphosgene is added, under an inert atmosphere at ambient temperature, to 0.2 g (0.6 mmol) of methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate in 10 ml of dioxane. After stirring for 10 minutes, 58 μl (1.2 mmol) of hydrazine hydrate and 0.4 ml (3 mmol) of triethylamine are added. The reaction medium is stirred for 3 hours and then hydrolysed with water. The aqueous phase is extracted with ethyl acetate. The organic phase obtained is dried over sodium sulphate, filtered, and then concentrated under reduced pressure. The solid obtained is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (95/5) mixture. 16 mg of a yellow solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859544B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-337cc1c81e154b41b37a65ca2023ad6b |
| Source note | uspto-grants-2014_10 |