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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091744Generated: November 1, 2026

Hydrazine hydrate (1:1) → 4-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)benzyl)-5,6,7-trimethyl-2,6-dihydro-1H-pyrrolo[3,4-d]pyridazin-1-one

https://huagongshe.com/reaction/1091744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantMethyl 4-(2-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)phenyl)acetyl)-1,2,5-trimethyl-1H-pyrrole-3-carboxylateHCID 57791825—
SolventAcetic AcidHCID 176—
Product4-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)benzyl)-5,6,7-trimethyl-2,6-dihydro-1H-pyrrolo[3,4-d]pyridazin-1-oneHCID 577918585.5%

Reaction Steps

Hydrazine hydrate (0.014 mL, 0.19 mmol) was added to methyl 4-(2-(4-fluoro-3-(4-methoxypiperidine-1-carbonyl)phenyl)acetyl)-1,2,5-trimethyl-1H-pyrrole-3-carboxylate (59) (0.076 g, 0.17 mmol) in acetic acid (4 mL). The resulting solution was stirred at room temperature for 2 days. The resulting mixture was evaporated to dryness and the residue was azeotroped with toluene to afford crude product, which was purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5μ silica, 19 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the desired compound (4.00 mg, 5.49% yield); m/z (LC-MS, ESI+), RT=1.60 min (M+H=427.11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129380B2
Source datasetuspto-grants-2012_03
ORD IDord-4d99762481d94fb68db470e87873f9af
Source noteuspto-grants-2012_03