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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231081Generated: November 1, 2026

HCID 18463943, compound → HCID 18463943, compound

https://huagongshe.com/reaction/2231081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18463943HCID 18463943—
ReactantHCID 22956506HCID 22956506—
ProductHCID 18463940HCID 18463940—
ProductHCID 18463943HCID 1846394335%

Reaction Steps

3-(2-(6-[(Isoquinoline-1-carbonyl)-amino]-3,7-dioxo-2-propyl-[1,2]diazepan-1-yl)-acetylamino)-4-oxo-butyric acid (11b) was prepared from isoquinoline-1-carboxylic acid {2-[(2-benzyloxy-5-oxo-tetrahydro-furan-3-ylcarbamoyl)-methyl]-3,7-dioxo-1-propyl-[1,2]diazepan-4-yl}-amide (10b, diastereomers) (95 mg, 0.16 mmol) by the method used to prepare 11a to afford 28 mg (35% yield) of the title compound. 1H-NMR (500 MHz, CDCl3/CD3OD=0.5 mL/3 drops) δ 0.90-1.00 (t, 3H), 1.65-1.80 (m, 2H), 2.10-2.28 (m, 1H), 2.32-2.40 (m, 1H), 2.47-2.80 (m, 3H), 3.05-3.18 (m, 1H), 3.30-3.51 (m, 2H), 4.00-4.55 (m, 3H), 5.10-5.20 (m, 1H), 7.75-8.05 (m, 4H), 8.49 (s, 1H), 8.90-9.00 (m, 1H). Analytical HPLC: 6.26 min. LC-MS (ES+): m/e=498 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426413B1
Source datasetuspto-grants-2002_07
ORD IDord-2930224274364e79b63ebd803621cda7
Source noteuspto-grants-2002_07