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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209576Generated: November 1, 2026

Ethoxyacetic acid → HCID 9932172, compound

https://huagongshe.com/reaction/2209576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxyacetic acidHCID 12301—
ReactantSodium HydroxideHCID 14798—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 57251661HCID 57251661—
SolventDichloromethaneHCID 6344—
ProductHCID 9932172HCID 993217286%

Reaction Steps

To a stirred solution of 4-amino-1-[(9S,10S)-2-chloro-9,10-dihydro-9,10-methanoanthracene-9-ylmethyl]piperidine (752 mg, 2.22 mmol), dimethylaminopyridine (542 mg, 4.44 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (848 mg, 4.44 mmol), in methylene chloride (15 mL) was added ethoxyacetic acid (0.25 mL, 2.44 mmol). After stirring for 18 h, the mixture was treated with 1N sodium hydroxide (75 mL), and extracted with methylene chloride (3×75 mL). The combined extracts were washed with 1N sodium hydroxide (2×75 mL) and brine (50 mL), dried (sodium sulfate), filtered and concentrated to give a milky white syrup. Chromatography of this material over silica gel (eluant: ethyl acetate) provided the title compound as a colorless glass (807 mg, 86%), mp 68.0°-70.0° C.; MS(CI): 425 (M+H); [α]D23 =+41° (c=0.01, CHCl3); NMR (300 MHz,DMSO-d6): 1.13(t, 3H, J=7.0 Hz), 1.49(m, 2H), 1.61(m, 2H), 2.26(m, 2H, J=11.9 Hz), 2.46(br s, 2H), 2.94(m, 2H), 3.33(m, part. submerged, 2H), 3.43(q, 2H, J=7.0 Hz), 3.62(m, 1H), 3.78(s, 2H), 4.33(s, 1H), 6.94(m, 3H), 7.23(br m, 4H), 7.48(d, 1H, J=8.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455246
Source datasetuspto-grants-1995_10
ORD IDord-2183ff6e6707408bace893a8433dca6f
Source noteuspto-grants-1995_10