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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301311Generated: November 1, 2026

HCID 22347460, compound → HCID 68787265, compound

https://huagongshe.com/reaction/2301311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22347460HCID 22347460—
ReactantHCID 22347482HCID 22347482—
ProductHCID 68787265HCID 6878726583%

Reaction Steps

834 mg (2.05 mmol) of 4-benzyloxycarbonylamino-3-t-butoxycarbonylbenzenesulfonamide and 783 mg (2.05 mmol) of benzyl 4-chloro-2-N-phenoxycarbonylanthranilate were treated in the same way as in Preparation Example 17 to obtain 1.18 g (yield 83%) of benzyl 2-{[(4-benzyloxycarbonylamino-3-t-butoxycarbonylbenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate. Properties: colorless amorphous, PMR (δ ppm, CDCl3): 1.56 (9H, s), 5.22 (2H, s), 5.37 (2H, s), 7.04 (1H, dd), 7.33-7.42 (10H, m), 7.97 (1H, d), 8.14 (1H, d), 8.45 (1H, d), 8.60 (1H, d), 8.65 (1H, d), 11.01 (1H, s), 11.11 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500835B2
Source datasetuspto-grants-2002_12
ORD IDord-9939ec6693cf49cc88eeaf94cd471739
Source noteuspto-grants-2002_12