HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899733Generated: October 30, 2026
Potassium Iodide → HCID 59694184, compound
https://huagongshe.com/reaction/899733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate | HCID 15829159 | — |
| Reactant | HCID 59694102 | HCID 59694102 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59694184 | HCID 59694184 | 12% |
Reaction Steps
A mixture of (2-imidazol-1-yl-ethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (92 mg, 0.37 mmol), 2-chloromethyl-benzimidazole-1-carboxylic acid tert-butyl ester (101 mg, 0.379 mmol), potassium iodide (3 mg, 0.02 mmol), and N,N-diisopropylethylamine (0.10 mL, 0.57 mmol) in acetonitrile (4 mL) was heated at 60° C. for 15 h. Saturated NaHCO3(aq) (15 mL) was added, and the mixture was extracted with CH2Cl2 (3×15 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (250:5:1 CH2Cl2/MeOH/NH4OH) gave a yellow oil (21 mg, 12%). 1H NMR (CDCl3) δ 1.45 (m, 1H), 1.66 (m, 10H), 1.91 (m, 2H), 2.69 (m, 2H), 2.92 (m, 1H), 3.18 (m, 1H), 3.67 (m, 2H), 4.20 (dd, 1H, J=10, 5.6 Hz), 4.67 (d, 1H, J=15 Hz), 4.80 (d, 1H, J=15 Hz), 6.74 (s, 1H), 6.90 (s, 1H), 7.01 (dd, 1H, J=7.7, 4.7 Hz), 7.73 (m, 1H), 7.86 (m, 1H), 8.38 (d, 1H, J=3.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354934B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-8b14258fc952445888ac0f72e48e7143 |
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| Source note | uspto-grants-2008_04 |
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