HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292205Generated: October 31, 2026
Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 10475248, compound
https://huagongshe.com/reaction/1292205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tricyclo(3.3.1.13,7)dec-1-ylmethylamine | HCID 86625 | — |
| Reactant | HCID 18660183 | HCID 18660183 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 10475248 | HCID 10475248 | 72.5% |
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 4N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756532 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-00f7753c137d40f0a5a0bc77779be696 |
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| Source note | uspto-grants-1998_05 |
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