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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231093Generated: November 1, 2026

HCID 18463938, compound → HCID 86758388, compound

https://huagongshe.com/reaction/2231093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18463938HCID 18463938—
ReactantHCID 54456005HCID 54456005—
ProductHCID 18463918HCID 18463918—
ProductHCID 86758388HCID 86758388100%

Reaction Steps

[6-(4-Allyloxy-3,5-dichloro-benzoylamino)-2-methanesulfonyl-7-oxo-[1,2]diazepan-1-yl]-acetic acid (25) was prepared from [6-(4-allyloxy-3,5-dichloro-benzoylamino)-2-methanesulfonyl-7-oxo-[1,2]diazepan-1-yl]-acetic acid tert-butyl ester (24) by the method used to prepare 8a to afford 173 mg (100% yield) of the title compound. 1H-NMR (500 MHz, CDCl3) δ 1.74-1.77 (m, 1H), 1.91-1.93 (m, 1H), 2.22-2.25 (m, 2H), 3.19 (s, 3H), 3.39-3.44 (m, 1H), 4.24-4.28 (m, 2H), 4.61-4.63 (m, 2H), 4.71-4.75 (d, 1H), 5.12-5.15 (m, 1H), 5.28-5.31 (m, 1H), 5.40-5.44 (m, 1H), 6.10-6.16 (m, 1H), 7.31-7.33 (d, 1H), 7.79 (s, 2H). Analytical HPLC: 5.70 min. LC-MS (ES+): m/e=494, 496 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426413B1
Source datasetuspto-grants-2002_07
ORD IDord-2871874ce8e745b8abd1f825aab053d7
Source noteuspto-grants-2002_07