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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896131Generated: November 2, 2026

Nitric Acid → Tert-butyl 9-nitro-6-oxo-1,2,4a,5,6,7-hexahydropyrazino[1,2-a][1,5]benzodiazepine-3(4h)-carboxylate

https://huagongshe.com/reaction/1896131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantWaterHCID 962—
Reactanttert-butyl 6-oxo-1,2,4a,5,6,7-hexahydropyrazino[1,2-a][1,5]benzodiazepine-3(4H)-carboxylateHCID 58284919—
SolventAcetic AcidHCID 176—
ProductTert-butyl 9-nitro-6-oxo-1,2,4a,5,6,7-hexahydropyrazino[1,2-a][1,5]benzodiazepine-3(4h)-carboxylateHCID 67249636—

Reaction Steps

Nitric acid (65% solution, 0.20 mL, 3.2 mmol) was added to a solution of Example 1C (1.0 g, 3.2 mmol) in acetic acid (5 mL) at room temperature. The solution was stirred for 3 hours, and then the reaction mixture was poured into water (200 mL). The precipitate was collected by filtration from the aqueous solution to afford the title compound. 1H NMR (300 MHz, DMSO-d6) d ppm 8.00 (dd, J=8.92, 2.58 Hz, 1 H), 7.79 (d, J=2.78 Hz, 1 H), 7.24 (d, J=9.12 Hz, 1 H), 3.86-4.10 (m, 2 H), 3.36-3.50 (m, 1 H), 3.20-3.29 (m, 1 H), 2.81-2.99 (m, 1 H), 2.62-2.77 (m, 1 H), 2.18 (d, J=13.48 Hz, 1 H); MS (APCI+) m/z 307 (M+H-tBu)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518933B2
Source datasetuspto-grants-2013_08
ORD IDord-18c6d34bb7464394956ea9fcb988ffc5
Source noteuspto-grants-2013_08