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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231082Generated: November 1, 2026

HCID 18463921, compound → HCID 18463943, compound

https://huagongshe.com/reaction/2231082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18463921HCID 18463921—
ReactantHCID 18463943HCID 18463943—
ProductHCID 18463943HCID 1846394374%
ProductHCID 18463946HCID 18463946—

Reaction Steps

3-{2-[6-(3,5-Dichloro-4-hydroxy-benzoylamino)-3,7-dioxo-2-propyl-[1,2]diazepan-1-yl]-acetylamino}-4-oxo-butyric acid (11c) was prepared from N-{2-[(2-benzyloxy-5-oxo-tetrahydro-furan-3-ylcarbamoyl)-methyl]-3,7-dioxo-1-propyl-[1,2]diazepan-4-yl}-3,5-dichloro-4-hydroxy-benzamide (10d, diastereomers) (30 mg, 0.05 mmol) by the method used to prepare 11a to afford 19 mg (74% yield) of the title compound. 1H-NMR (500 MHz, CDCl3/CD3OD=0.5 mL/3 drops) δ 0.90-0.95 (t, 3H), 1.60-1.70 (m, 2H), 2.00-2.10 (m, 1H), 2.25-2.36 (m, 1H), 2.48-2.82 (m, 3H), 2.98-3.10 (m, 1H), 3.20-3.35 (m, 1H), 3.90-4.50 (m, 4H), 4.95-5.08 (m, 1H), 7.62-7.72 (m, 2H). Analytical HPLC: 5.40 min. LC-MS (ES+): m/e=531, 533 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426413B1
Source datasetuspto-grants-2002_07
ORD IDord-2634141a7c7042a9898bc1f5836963fe
Source noteuspto-grants-2002_07