HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132822Generated: October 30, 2026
Potassium Carbonate → {5-[3-(2-Aza-bicyclo[3.1.0]hex-2-yl)-propoxy]-1H-indol-2-yl}-morpholin-4-yl-methanone
https://huagongshe.com/reaction/132822
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Azabicyclo[3.1.0]hexane hydrochloride | HCID 67358156 | — |
| Reactant | [5-(3-Chloro-propoxy)-1H-indol-2-yl]-morpholin-4-yl-methanone | HCID 67527317 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | {5-[3-(2-Aza-bicyclo[3.1.0]hex-2-yl)-propoxy]-1H-indol-2-yl}-morpholin-4-yl-methanone | HCID 16754252 | 9.5% |
Reaction Steps
A mixture of 2-aza-bicyclo[3.1.0]hexane hydrochloride (example 4 step 7, 49 mg, 1.2 eq.) and potassium carbonate (118 mg, 2.5 eq.) in acetonitrile was stirred 1 h at 60° C. The reaction mixture was cooled to 30° C. and [5-(3-chloro-propoxy)-1H-indol-2-yl]-morpholin-4-yl-methanone (example 4, step 3, 110 mg, 1.0 eq.) was added. The resulting mixture was stirred 24 h at 80° C. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with an aqueous solution of sodium hydrogencarbonate and water and dried over sodium sulphate and evaporated in vacuo. The residue was purified on silica, eluting with a 98:2 to 9:1 gradient of dichloromethane/methanol, to yield 12 mg (8%) of the desired product as light yellow solid. MS (m/e): 370.4 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07388095B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-b63192ca715d46cca4cf20bad06bcf06 |
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| Source note | uspto-grants-2008_06 |
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