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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651327Generated: October 31, 2026

Sodium hydride → HCID 86757267, compound

https://huagongshe.com/reaction/651327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
ReactantHCID 18476664HCID 18476664—
SolventDimethylformamideHCID 6228—
ProductHCID 86757267HCID 8675726793%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of N-(diphenylmethylene)glycine t-butyl ester (1.30 g, 4.40 mmol) in 10 mL of DMF is treated with sodium hydride (60% in mineral oil, 0.250 g, 6.25 mmol) at 25° to give a red orange solution. After 1 h, the temperature is raised to 60° C. and a solution of the title B compound, 3-(4-iodobutyl)-1,2,3,4-tetrahydro-1-methyl-2,4-dioxoquinazoline (1.58 g, 4.41 mmol) in 10 mL of DMF is added dropwise over 10 min. After stirring for 5 h at 60° C. and 58 h at 25° C. the solvent is evaporated under reduced pressure, and the residue is partioned between 75 mL of ethyl acetate and 25 mL of water. The organic solution is washed with three 25 mL portions of brine, dried over anhydrous MgSO4, and concentrated to give 2.15 g of 2-(benzhydrylideneamino)-6-(1,2,3,4-tetrahydro-1-methyl-2,4-dioxoquinazolin-3-yl)hexanoic acid t-butyl ester as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277987B1
Source datasetuspto-grants-2001_08
ORD IDord-ab264d49398e480bae2c9d288e0fa6a7
Source noteuspto-grants-2001_08