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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258660Generated: November 2, 2026

Pyridine → HCID 135838164, compound

https://huagongshe.com/reaction/2258660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 135838149HCID 135838149—
SolventBenzeneHCID 241—
ProductHCID 135838164HCID 135838164—

Reaction Steps

N-(8-Bromo-1,2,5,6-tetrahydro-9-nitro-1-oxobenzo[f]quinazolin-3-yl)pivalamide (0.23 g, 0.5 mmole) was reacted with N-bromosuccinimide (0.12 g, 0.7 mmole) and pyridine (0.06 ml, 0.8 mmole) in dry benzene (150 ml) in the same manner as in example 2. The crude product was purified by trituration with methanol:water (1:9), followed by filtration and washing (water and methanol) to give, after drying, N-(8-bromo-1,2-dihydro-9-nitro-1-oxobenzo[f]quinazolin-3-yl)pivalamide as a pale yellow solid. (0.20 g, 94%) 1H NMR(DMSO-d6, 200 MHz) δ: 1.27(s, 9H, t-butyl); 7.76(d, J=9.0 Hz, 1H, Ar); 8.32(d, J=9.0 Hz, 1H, Ar); 8.65(s, 1H, Ar); 10.21(s, 1H, Ar); 11.40(s, 1H, NH); 12.45(br s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661155
Source datasetuspto-grants-1997_08
ORD IDord-74cf662c01ff4a879894286d53f7b203
Source noteuspto-grants-1997_08