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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373525Generated: October 26, 2026

Water → HCID 86600976, compound

https://huagongshe.com/reaction/1373525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonic AcidHCID 6395—
Reactant1[n-[(1,3-Benzodioxol-5-yl)sulfonyl]-n-(2-methylpropyl)amino]-3(s)-[bis(phenylmethyl)amino]-4-phenyl-2(r)-butanolHCID 11387841—
CatalystPalladium hydroxideHCID 9942167—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86600976HCID 86600976—

Reaction Steps

Part B: To the THF solution of crude 1-[N-[(1,3-benzodioxol-5-yl) sulfonyl]-N-(2-methylpropyl)amino]-3(S)-[bis(phenylmethyl)amino]-4-phenyl-2(R)-butanol was added water (500 mL) followed by methane sulfonic acid (531 g, 5.5 moles). The solution was stirred to insure complete mixing and added to a 5 gallon autoclave. Pearlman's catalyst (200 g of 20% Pd(OH)2 on C/50% water) was added to the autoclave with the aid of THF (500 mL). The reactor was purged four times with nitrogen and four times with hydrogen. The reactor was charged with 60 psig of hydrogen and stirring at 450 rpm started. After 16 hours, HPLC analysis indicated that a small amount of the mono-benzyl intermediate was still present. Additional catalyst (50 g) was added and the reaction was allowed to run overnight. The solution was then filtered through celite (500 g) to remove the catalyst and concentrated under vacuum in five portions. To each portion, toluene (500 mL) was added and removed under vacuum to azeotropically removed residual water. The resulting solid was divided into three portions and each washed with methyl t-butyl ether (2 L) and filtered. The residual solvent was removed at room temperature in a vacuum oven at less than 1 torr to yield the 2714 g of the expected salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07161033B2
Source datasetuspto-grants-2007_01
ORD IDord-1a1b9d8ba78d49d1ad982e9371cbef40
Source noteuspto-grants-2007_01