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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396495Generated: November 1, 2026

Triethylamine → n-Butyl(S)-3-[(6-oxo-1,6-dihydro-pyridazine-4-carbonyl)-amino]-tetrahydrofuran-3-carboxylate

https://huagongshe.com/reaction/1396495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant6-Oxo-1,6-dihydropyridazine-4-carboxylic acidHCID 12376265—
ReactantButyl (S)-3-aminotetrahydrofuran-3-carboxylateHCID 59621155—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Productn-Butyl(S)-3-[(6-oxo-1,6-dihydro-pyridazine-4-carbonyl)-amino]-tetrahydrofuran-3-carboxylateHCID 6802375790%

Reaction Steps

A solution of 6-oxo-1,6-dihydro-pyridazine-4-carboxylic acid (11.5 g), TBTU (25.3 g), triethylamine (20.9 mL) and 40 mL DMF in 200 mL THF was stirred for 30 minutes at ambient temperature. Then n-butyl (S)-3-amino-tetrahydrofuran-3-carboxylate (14.0 g) was added and the mixture was stirred further overnight. For working up the mixture was evaporated to dryness in vacuo and the residue was stirred with 200 mL of ethyl acetate. This solution was washed twice with 5% sodium hydrogen carbonate solution, then dried and evaporated down. The product was thus obtained in a yield of 90% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901127B2
Source datasetuspto-grants-2014_12
ORD IDord-9c2df8e642954f09a83020ff72633e89
Source noteuspto-grants-2014_12