HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400446Generated: November 1, 2026
Potassium Hydroxide → HCID 59455152, compound
https://huagongshe.com/reaction/1400446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 67310629 | HCID 67310629 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 59455152 | HCID 59455152 | — |
Reaction Steps
1-(8-Methoxy-2-methyl-2,3,4,4a-tetrahydro-1H-pyrido[4,3-b]indol-5(9bH)-yl)-2-(pyridin-4-yl)propan-2-ol (500 mg, 1.4 mmol) was dissolved in thionylchloride (5 mL) was stirred at RT for 2 h. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in N-methyl-2-pyrrolidone (4 mL) and stirred for 5 min. Powdered KOH (798 mg, 14.2 mmol) was added and stirring was continued at RT for additional 5 min. The reaction mixture was heated at 100° C. for 1 h. The progress of reaction was monitored by TLC and NMR. The reaction mixture was cooled at RT, diluted with water and extracted with EtOAc. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated and purified the compound by HPLC. 1H NMR (CD3OD, TFA salt) δ (ppm): 8.25 (d, 2H), 7.0 (m, 4H), 6.90 (d, 1H), 6.70 (d, 1H), 3.90 (m, 2H), 3.80 (s, 3H), 3.0 (t, 2H), 2.70 (s, 3H), 2.62 (m, 2H), 1.95 (s, 3H).
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-629b63edd8774270bfacbcf18d397676 |
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| Source note | uspto-grants-2014_12 |
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