HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → HCID 22912929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-fluoro-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 10103503 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22912929 | HCID 22912929 | — |
Reaction Steps
To a mixture of 1.97 g of 6-fluoro-1,2,3,4-tetrahydroquinoxalin-2-one (EXAMPLE 6), 3.1 ml of diisopropylethylamine, and 11 ml of THF is added 1.4 ml of methyl chloroformate. The reaction is cooled with cool tap water as an exotherm ensued. After 35 min, the mixture is partitioned between ethyl acetate, aq. sodium bicarbonate, and saline. The organic layers are dried over magnesium sulfate, concentrated, and the crude product is crystallized from dichloromethane/methanol/ethyl acetate to give 2.06 g of methyl 6-fluoro-1,2,3,4-tetrahydro4-(methoxycarbonyl)quinoxaline-2-one; mp 206.5°-207.5°; NMR (CDCl3) 3.86, 4.43, 6.84, 7.48, 8.67 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541324 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-873cdf74cb314cf7977834ad21c7fe58 |
| Source note | uspto-grants-1996_07 |