HCID 14299925, compound → HCID 11658392, compound

HRID 467148Notes

Reaction equation

HRID 467148 reaction equation
[CH3:1][O:2][CH:3]([O:16][CH3:17])[C@@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1C(OC(C)(C)C)=O.[ClH:18].CO>>[ClH:18].[CH3:1][O:2][CH:3]([O:16][CH3:17])[C@@H:4]1[CH2:8][CH2:7][CH2:6][NH:5]1

Participants

3

Procedure

tert-Butoxycarbonyl-L-prolinal dimethyl acetal (1.0 g, 4.08 mmol) is stirred for one hour at room temperature in 10% HCl-methanol (8.2 ml) and the mixture is evaporated to dryness under reduced pressure to give quantitatively L-prolinal dimethylacetal hydrochloride as a solid. The product is dissolved in dimethylformamide (5 ml) containing p-anisic acid (938 mg, 6.16 mmol) and diethyl-phosphoryl cyanide (0.65 ml, 8.25 mmol). To the solution is added dropwise triethylamine (1.15 ml, 8.25 mmol) under cooling and agitation in an ice-methanol bath. After the dropwise addition the mixture is stirred for one hour under cooling and then for one hour at room temperature. Benzene-ethyl acetate (2:1, 150 ml) is added to the reaction mixture and the organic layer was separated, washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml) and a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate and filtered. The filtrate is concentrated to dryness under reduced pressure. The residue is purified by column chromatography on silica gel (n-hexane-dichloromethanemethanol, 6:4:1) to give 747 mg (65%) of the title compound as white crystals.

Workup

  1. customthe mixture is evaporated to dryness under reduced pressure

Sources & evidence

ORD record
ord-18d09b3d7ba74b7881f1434751a86429
Source dataset
uspto-grants-1992_10
Patent number
US05158970

Reaction notes

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