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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071592Generated: November 3, 2026

P-Anisidine → Benzamide

https://huagongshe.com/reaction/1071592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHCID 10755041HCID 10755041—
ProductBenzamideHCID 233156.3%

Reaction Steps

The title compound was synthesized as in Example 1 using p-anisidine (1.0 g, 7.1 mmol), CSI (0.85 mL, 9.8 mmol), and 3-amino-N-(3,4-difluoro-phenyl)-4-methoxy-benzamide (1.75 g, 6.3 mmol) to give 0.43 g of benzamide, N-(3,4-difluorophenyl)-4-methoxy-3-[[[[[(4-methoxyphenyl)amino]-carbonyl]amino]sulfonyl]amino]-. Microanalysis: C22H20F2N4O6S; calculated: C=52.17; H=3.98; N=11.06. found: C=52.17; H=3.89; N=10.95. Mp 189-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906094B2
Source datasetuspto-grants-2005_06
ORD IDord-e20c99807d2b4d91a40fb64611e937b0
Source noteuspto-grants-2005_06