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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726465Generated: October 31, 2026

Water → HCID 59656362, compound

https://huagongshe.com/reaction/1726465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantIsopropyl isocyanateHCID 61277—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 86594773HCID 86594773—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59656362HCID 59656362—

Reaction Steps

(±)-(cis)-1-Butyryl-4-[4-(2-methyl-benzoylamino)-naphthalene-1-sulfonylamino]-piperidine-3-carboxylic acid ethyl ester was made following general procedure in Scheme 5, substituting (±)4-amino-1-benzyl-piperidine-3-carboxylic acid ethyl ester (5) for 4-amino-piperidine-1-carboxylic acid tert-butyl ester and substituting butyl chloride for 2-isocyanato-propane. To the solution of (±)-(cis)-1-butyryl-4-[4-(2-methyl-benzoylamino)-naphthalene-1-sulfonylamino]-piperidine-3-carboxylic acid ethyl ester (70 mg, 0.12 mmol) in THF (5 mL), was added lithium hydroxide in water solution (6 mg, 0.25 mmol) and the resultant solution was stired at 25° C. for 2 h. The reaction mixture was extracted with CH2Cl2. The organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated to provide the crude product. HPLC purification of the residue gave the title compound. 1H NMR (300 MHz, DMSO) δ 10.62 (s, 1H), 8.77 (t, 1H), 8.24 (m, 3H), 7.95 (d, 1H), 7.70 (m, 3H), 7.38 (m, 3H), 3.72 (m, 2H), 3.35 (m, 6H), 3.12 (m, 1H), 2.60 (m, 1H), 2.15 (m, 2H), 1.32 (m, 4H), 0.80 (dd, 3H); LC/MS nm/z 539 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491827B2
Source datasetuspto-grants-2009_02
ORD IDord-3247586c2d114f3eaf1abf822757a91d
Source noteuspto-grants-2009_02