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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384711Generated: November 2, 2026

Phosgene → HCID 22954557, compound

https://huagongshe.com/reaction/1384711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Benzyl 3-tert-butyl (3S)-tetrahydropyridazine-1,3(2H)-dicarboxylateHCID 11034558—
ReactantHCID 18465756HCID 18465756—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 22954557HCID 2295455789%

Reaction Steps

A solution of (35)-1-benzyl 3-t-butyl hexahydropyridazine-1,3-dicarboxylate (Hassall et al. J. Chem. Soc. Perkin 1, pp. 1451-1454 (1979)) (925.3 mg, 2.89mmol) and disopropylethylamine (0.70 ml, 4.0 mmol) in a 1.93M toluene solution of phosgene (17.96 ml, 34.7 mmol) was stirred at room temperature for 45 min, then concentrated to leave a yellow solId. To this solid was added toluene (18 ml), hydrazide (259) (861.6 mg, 2.89 mmol) and diisopropylethylamine (0.70 ml, 4.0 mmol). The mixture was stirred at room temperature for 2.75 h, then concentrated. The resulting residue was taken up in EtOAc, washed twice with 1M HCl, brine, then dried (MgSO4), filtered and concentrated to afford 2.15 g of crude material. Flash chromatography (40% EtOAc in hexane) afforded 1.65 g (89%) of the title compound as a white foam: mp 40° C.; [α]D24 −55.78 (c 0.40, CH2Cl2); IR (KBr) 3436, 2930, 1733, 1689, 1455, 1412′ 1367, 1258, 1156, 697; 1H NMR (CDCl3) δ 8.54-8.23 (0.5H, m), 7.97-7.09 (15.5H), 5.16-4.80 (4H, m), 4.66-4.32 (1H, m), 4.24-3.55 (3.3H, m), 3.50-3.26 (0.4H, m), 3.19-2.49 (2.3H, m), 2.11-1.43 (6H, m), 1.32-1.05 (7H, m);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258948B1
Source datasetuspto-grants-2001_07
ORD IDord-9b0de6cecfb54800b7c551a583ceae9c
Source noteuspto-grants-2001_07