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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654354Generated: November 4, 2026

Pyridine → HCID 135838164, compound

https://huagongshe.com/reaction/1654354

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 numberUS05405851
Source datasetuspto-grants-1995_04
ORD IDord-fd6ee30403b443e2bdf51dc2ce1f2a54
Source noteuspto-grants-1995_04