HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899715Generated: October 31, 2026
Trimethylsilyl isocyanate → HCID 59694160, compound
https://huagongshe.com/reaction/899715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | HCID 10126165 | HCID 10126165 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 59694160 | HCID 59694160 | — |
Reaction Steps
A solution of (1H-benzimidazol-2-ylmethyl)-piperidin-4-yl-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (0.16 g, 0.43 mmol) in isopropanol (3 mL) was treated with trimethylsilylisocyanate (81 μL, 0.60 mmol) at room temperature. The reaction was stirred 20 hours and concentrated under reduced pressure. This afforded, after column chromatography with silica gel (5:0.5:94.5 MeOH:NH4OH:CH2Cl2), 4-[(1H-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amino]-piperidine-1-carboxylic acid amide (112 mg, 66%). 1H NMR (CDCl3) δ 1.42 (m, 1H), 1.60-1.95 (m, 5H), 2.02 (br, 1H), 2.24 (br, 1H), 2.60-2.80 (m, 4H), 2.89 (m, 1H), 3.70 (br, 1H), 4.03 (br, 1H), 4.15 (m, 3H), 4.39 (br, 2H, NH2), 7.18 (m, 3H), 7.45 (d, 1H, J=7.5 Hz), 7.66 (br, 2H), 8.59 (d, 1H, J=4.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354932B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-69e52c2b1bd74a4fa78c819900e1626a |
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| Source note | uspto-grants-2008_04 |
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