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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720488Generated: October 31, 2026

Diisopropylamine → HCID 70050443, compound

https://huagongshe.com/reaction/1720488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzyl 2-(2-formylpyrrolidine-1-carbonyl)pyrrolidine-1-carboxylateHCID 122623—
Reactant(S)-(-)-Methyl p-tolyl sulfoxideHCID 11170275—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70050443HCID 7005044388.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To diisopropylamine (0.26 ml) in THF (6 ml) was dropwise added 1.62M n-butyllithium-hexane solution (1.12 ml) at -78° C., and the mixture was stirred at 0° C. for 0.5 hour. The reaction mixture was cooled to -30° C., dropwise added with (S)-(-)-methyl p-tolyl sulfoxide (255 mg) in THF (6 ml), and stirred at 0° C. for 0.5 hour. The reaction mixture was cooled to -78° C. and dropwise added with known N-benzyloxycarbonyl-L-prolyl-L-prolinal (300 mg) in THF (6 ml). After stirring for 0.5 hour, an aqueous solution of saturated ammonium chloride was added thereto, followed by stirring at room temperature for 10 minutes. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with a saturated aqueous solution of sodium bicarbonate and saturated brine order, dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (eluate; chloroform-methanol) to give 388 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506256
Source datasetuspto-grants-1996_04
ORD IDord-3e6f706c851e499eb3d97ef7385fee51
Source noteuspto-grants-1996_04