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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435911Generated: November 1, 2026

HCID 22347460, compound → HCID 22557533, compound

https://huagongshe.com/reaction/1435911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22347460HCID 22347460—
ReactantHCID 22347489HCID 22347489—
ProductHCID 22557533HCID 2255753393.1%

Reaction Steps

320 mg (1.17 mmol) of 3-t-butoxycarbonyl-4-hydroxybenzenesulfonamide and 447 mg (1.17 mmol) of benzyl 4-chloro-2-N-phenoxycarbonylanthranilate were treated in the same way as in Preparation Example 17 to obtain 611 mg (yield 93%) of benzyl 2-{[(3-t-butoxycarbonyl-4-hydroxybenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate. Properties: colorless amorphous, PMR (δ ppm, CDCl3): 1.62 (9H, s), 5.35 (2H, s), 7.01-7.05 (2H, m), 7.37-7.41 (5H, m), 7.96 (1H, d), 8.10 (1H, dd), 8.46-8.48 (2H, m), 10.99 (1H, s), 11.66 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618977B2
Source datasetuspto-grants-2009_11
ORD IDord-2310add92bd2428daabe91a19a8fc999
Source noteuspto-grants-2009_11