Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444752Generated: October 29, 2026

Water → HCID 22260271, compound

https://huagongshe.com/reaction/444752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22260270HCID 22260270—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22260271HCID 22260271—

Reaction Steps

To a solution of 5-(4,4-dimethyl-2-oxo-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1,4-dimethyl-1H-pyrrole-2-carbonitrile (1 eq, 0.15 g, 0.51 mmol) in THF (5 mL) at −78° C. was added N-bromosuccinimide (1.1 eq, 0.1 g, 0.56 mmol). The solution was allowed to warm and stir for 16 hours. Pyridine (1 mL) was added and the mixture was poured into water (15 mL), the layers were separated, the aqueous layer was extracted with ethyl acetate (3×10 mL) and the combined organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The product, 5-(4,4-dimethyl-2-oxo-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-3-bromo-1,4-dimethyl-1H-pyrrole-2-carbonitrile was obtained by crystallization from 20% ethyl acetate/hexane as a white crystalline solid. 1H NMR (300 MHz, d6-DMSO): δ 1.64 (s, 6H), 1.93 (s, 3H), 3.57 (s, 3H), 7.01 (d, 1H, J=8 Hz), 7.31 (dd, 1H, J=1.95, 8 Hz), 7.35 (s, 1H), 10.43 (s, 1H). MS m/z (ESI (−)) 372/374 (M−H)−. Anal. calcd for C17H16N3O2, C, 54.6, H, 4.31; N, 11.2. Found, C, 54.8, H, 4.42; N, 11.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476262B2
Source datasetuspto-grants-2013_07
ORD IDord-416f871ba3324f5591c0ed25ee3c4187
Source noteuspto-grants-2013_07