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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282304Generated: November 1, 2026

P-Anisidine → HCID 10111456, compound

https://huagongshe.com/reaction/1282304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHCID 10805016HCID 10805016—
ProductHCID 10111456HCID 10111456—

Reaction Steps

Prepared from 2,3-dimethoxy-6-methyl-7-nitro-quinoxaline-5-carbonyl chloride (13) 250 mg (0.80 mmol) and 4-anisidine 207 mg (1.68 mmol). Reaction was continued for 24 hours, and the crude product was eluted through a flash column (3:2 hexanes:ethyl acetate), 210 mg (66%), mp 206-208° C.; 1H NMR (CDCl3): δ 8.33 (s, 1H), 7.71 (d, 2H, J=9.0 Hz), 7.60 (s, 1H), 6.88 (d, 2H, J=8.8 Hz), 4.16 (s, 3H), 4.00 (s, 3H), 3.79 (s, 3H), 2.57 (s, 3H); MS (APCI): m/z 399 (M+H). Anal. Calcd. for C19H18N4O6: C, 57.29; H, 4.55; N, 14.06. Found: C, 57.23; H, 4.73; N, 14.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455698B1
Source datasetuspto-grants-2002_09
ORD IDord-6a74a49f173446c9b865a7b2fced4731
Source noteuspto-grants-2002_09