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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864935Generated: November 1, 2026

Hydrochloric Acid → Ammonium Hydroxide

https://huagongshe.com/reaction/1864935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHOAtHCID 181649—
ReactantMethyl 1-{[(3S)-3-amino-3-phenylpropyl]amino}cyclopentanecarboxylate bis-hydrochlorideHCID 66973378—
SolventTetrahydrofuranHCID 8028—
ProductAmmonium HydroxideHCID 14923—
Product(9S)-9-phenyl-6,10-diazaspiro[4.6]undecan-11-oneHCID 66973323—

Reaction Steps

Potassium trimethylsilanoate (1.21 g, 9.45 mmol) was added to a stirred suspension of methyl 1-{[(3S)-3-amino-3-phenylpropyl]amino}cyclopentanecarboxylate bis-hydrochloride (1.00 g, 2.86 mmol, Intermediate 38) in THF (5.0 mL) at ambient temperature. After 4 h, the reaction mixture was adjusted to pH=8 with aqueous 1 M HCl. To this mixture was added HOAt (0.195 g, 1.43 mmol), and EDCI (0.549 g, 2.87 mmol). After 1 h, the reaction was concentrated in vacuo. The residue was partitioned between CH2Cl2 and water. The aqueous phase was extracted several times with CH2Cl2. The combined organic extracts were washed with saturated brine, then dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography, eluting with CH2Cl2:MeOH:NH4OH-89.9:10:0.1 to give the title compound. MS: m/z=245 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625901B2
Source datasetuspto-grants-2009_12
ORD IDord-81e60206e29c4ddbb93257f32d7b9a09
Source noteuspto-grants-2009_12