HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isocyanoacetate → tert-Butyl (S)-12,12a-dihydroimidazo[1,5-a]pyrrolo[2, 1-c]quinoxaline-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isocyanoacetate | HCID 2759404 | — |
| Reactant | (S)-3,3a-Dihydropyrrolo(1,2-a)quinoxaline-1,4(2H,5H)-dione | HCID 10104293 | — |
| Product | tert-Butyl (S)-12,12a-dihydroimidazo[1,5-a]pyrrolo[2, 1-c]quinoxaline-1-carboxylate | HCID 53953867 | — |
Reaction Steps
Following the general procedure of EXAMPLE 30 and making non-critical variations but starting with (S)-3,3a-dihydropyrrolo[1,2-a]quinoxaline-1,4(2H,5H)-dione (intermediate formed in EXAMPLE 282, 0.638 g) and tert-butyl isocyanoacetate (0.621 g), the title compound is obtained, mp 202°-207° (decomp); MS (m/z) at 325; IR (mineral oil) 1719, 1363, 1700, 1507, 1161, 1293 cm-1 ; NMR (CDCl3) 1.64, 2.25-2.40, 2.55-2.81, 3.31-3.41, 5.26, 7.23-7.29, 7.33, 7.52, 8.06, 8.34 δ; [α]D =-248° (0.96, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574038 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-04913cf4be094362a6920062d0d2ca05 |
| Source note | uspto-grants-1996_11 |