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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230425Generated: November 1, 2026

N-(2-Benzyloxy-5-oxotetrahydrofuran-3-yl)-6,10-dioxo-octahydro-9-(3-phenylpropionylamino)-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxamide → 3-(6,10-Dioxo-octahydro-9-(3-phenylpropionylamino)-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxamido)-4-oxobutanoic acid

https://huagongshe.com/reaction/2230425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Benzyloxy-5-oxotetrahydrofuran-3-yl)-6,10-dioxo-octahydro-9-(3-phenylpropionylamino)-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxamideHCID 18465764—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-(6,10-Dioxo-octahydro-9-(3-phenylpropionylamino)-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxamido)-4-oxobutanoic acidHCID 18465692—

Reaction Steps

A mixture of [3S,2R,S, (1S,9S)] N-(2-benzyloxy-5-oxotetrahydrofuran-3-yl)-6,10-dioxo-octahydro-9-(3-phenylpropionylamino)-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxamide (46a) (205 mg; 0.364 mmol), 10% palladium on carbon (200 mg) and methanol (20 ml) was stirred under hydrogen at atmospheric pressure for 5 h. The mixture was filtered then concentrated to yeild 154 mg (90%) of a glass: mp. 116-118° C.; [α]D23 −140° (c 0.1, CH3OH); IR (KBr) 3323 (br), 1783, 1731, 1658, 1539, 1455, 1425; 1H NMR (CD3OD) δ7.21 (5H, m), 5.17 (1H, m), 4.73 (1H, m), 4.50 (2H, m), 4.23 (1H, m), 3.38 (1H, m), 3.06 (1H, m), 2.91 (2H, m), 2.73-2.18 (6H, m) and 2.01-1.59 (5H, m). Anal. Calcd for C23H27N4O7+H2O: C, 56.32; H, 6.16; N, 11.42. Found: C, 56.29; H, 6.11; N, 11.25. MS(FAB, m/z) 473 (M++1), 176, 149, 105, 91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423840B1
Source datasetuspto-grants-2002_07
ORD IDord-a445e3c60e3f420aab097e206b452fdf
Source noteuspto-grants-2002_07