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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760160Generated: October 31, 2026

Triphenylphosphine → 3-{[Methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-methyl}-pyridine-2-carboxylic Acid Isopropyl Ester

https://huagongshe.com/reaction/1760160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 2-(4-methylphenylsulfonamido)acetateHCID 562880—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantPropan-2-yl 3-(hydroxymethyl)pyridine-2-carboxylateHCID 22346407—
SolventTetrahydrofuranHCID 8028—
Product3-{[Methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-methyl}-pyridine-2-carboxylic Acid Isopropyl EsterHCID 59983160—

Reaction Steps

Isopropyl 3-(hydroxymethyl)pyridine-2-carboxylate (prepared in accordance with P. Ornstein et. al. J. Med. Chem. 1989, 32, 827) (200 g, 1.02 mol), methyl N-[(4-methylphenyl)sulfonyl]glycinate (249 g, 1.02 mol), and triphenylphosphine (403 g, 1.5 mol) were dissolved in dry THF (3000 mls) and cooled to zero degrees under N2. The diethylazodicarboxylate (DEAD) (267.6 g, 1.5 mol) was dissolved in dry THF (250 mls) and placed in a 500 ml addition funnel. The DEAD was added dropwise over 1 hour. The ice bath was removed and the reaction was allowed to warm slowly to RT. After 2 hours, the reaction was checked by HPLC (above conditions) and some glycinate remained. More starting reagents were added and the reaction was left to stir at RT. After 30 min, the reaction was checked again and saw a very small amount of the glycinate remaining. Concentrated reaction down to a reddish-orange oil that was carried onto the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841558B2
Source datasetuspto-grants-2005_01
ORD IDord-d75fb16893d04578abbf3eb6b2a7cfdf
Source noteuspto-grants-2005_01