HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400473Generated: November 3, 2026
Potassium Phosphate, Tribasic → HCID 59455166, compound
https://huagongshe.com/reaction/1400473
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 2,3,4,5-tetrahydro-8-isopropyl-2-methyl-1H-pyrido[4,3-b]indole | HCID 59455219 | — |
| Reactant | (E)-4-(1-bromoprop-1-en-2-yl)pyridine | HCID 86642478 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59455166 | HCID 59455166 | — |
Reaction Steps
8-Isopropyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (150 mg, 0.65 mmol) was dissolved in DMF. Copper (I) iodide (14 mg, 0.074 mmol), L-proline (17 mg, 0.015 mmol) and potassium phosphate (340 mg, 1.48 mmol) were added and the reaction mixture was stirred for 10 min. at RT. 4-(1-Bromoprop-1-en-2-yl)pyridine (220 mg, 0.9 mmol) was added dropwise and the reaction mixture was purged with nitrogen. The reaction mixture was heated overnight at 85° C. (prolonged heating in some cases was required). DMF was evaporated under reduced pressure, the residue was diluted with water and the solid was filtered. The solid material was purified by silica gel chromatography (100-200 mesh). The product was further purified by HPLC. 1H NMR (CD3OD, TFA salt) δ (ppm): 8.80 (d, 2H), 8.20 (d, 2H), 7.70 (s, 1H), 7.40 (s, 1H), 7.20 (m, 2H), 4.40 (m, 1H), 3.90 (m, 1H), 3.70 (m, 1H), 3.22 (m, 3H), 3.15 (s, 3H), 3.0 (m, 1H), 2.10 (s, 3H), 1.30 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906925B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c1372ace6e784dfaa2f8d7fc3f349c25 |
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| Source note | uspto-grants-2014_12 |
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