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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984010Generated: October 29, 2026

HCID 22347460, compound → HCID 22557541, compound

https://huagongshe.com/reaction/984010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22347460HCID 22347460—
ReactantHCID 22347461HCID 22347461—
ProductHCID 22557541HCID 2255754162%

Reaction Steps

960 mg (3.00 mmol) of 3-benzyloxycarbonylamino-4-methylbenzenesulfonamide and 1.14 g (3.00 mmol) of benzyl 4-chloro-2-N-phenoxycarbonylanthranilate were treated in the same way as in Example 8 to obtain 1.14 g (yield 62% of benzyl 2-{[(3-benzyloxycarbonylamino-4-methylbenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate. Properties: colorless amorphous, PMR (δ ppm, DMSO-d6): 2.30 (3H, s), 5.17 (2H, s), 5.36 (2H, s), 7.20 (1H, dd), 7.33-7.48 (1H, m), 7.63 (1H, d), 7.97 (1H, d), 8.11 (1H, s), 8.25 (1H, s), 9.27 (1H, s), 10.30 (1H, s), 12.20 (1H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867214B1
Source datasetuspto-grants-2005_03
ORD IDord-02c75cb0d8b040b8a2fe5986784a91e4
Source noteuspto-grants-2005_03