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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737422Generated: November 2, 2026

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 10475248, compound

https://huagongshe.com/reaction/1737422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
ReactantHCID 18660183HCID 18660183—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 10475248HCID 1047524872.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

(R)-2-(Toluene-4-sulfonyloxymethyl)-6-fluoro-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-one (1.0 g, 2.5 mmole) and 1-adamantylmethylamine (1.6 g, 10 mmole) were combined in 30 ml of dry DMSO and heated at 80-90° C. for 4 hours under an argon atmosphere. After cooling to room temperature, the mixture was diluted with 500 ml of 1:1 ethyl acetate/hexane and washed with 250 ml of saturated aqueous sodium bicarbonate and with two 250 ml portions of water, dried over sodium sulfate, filtered and concentrated in vacuum. The residue was column chromatographed on silica gel using 0.5% methanol/CHCl3 as eluant to give 0.70 g of the free base of the title compound as a colorless oil. This was crystallized from ethanol with the addition 4 N isopropanolic HCl to give 0.54 g of the (S) enantiomer of the title compound as a fluffy white solid hydrochloride, m.p.>260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962465
Source datasetuspto-grants-1999_10
ORD IDord-b90b0b5068904a9b87130e1c802c8e00
Source noteuspto-grants-1999_10