HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 131720707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 131720708 | HCID 131720708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Product | HCID 131720707 | HCID 131720707 | — |
Reaction Steps
274 mg of methyl [(S)-3-[(S)-3-[cyclopropyl-(3-hydroxypropyl)-carbamoyl]-2-(naphthalen-2-ylsulfonylamino)-propionylaminomethyl]-piperidin-1-yl]-imino-methylcarbamate (Example 63), 1 ml of 1N methyl iodide in THF, 2 ml of 1 molar DBU solution in THF and 2 ml of methylene chloride are stirred together at room temperature. The mixture is concentrated and the residue is chromatographed over silica gel with ethyl acetate-methanol 9:1. There are obtained 120 mg of (S)-N1-cyclopropyl-N4-[(S)-1-(iminomethoxycarbonylamino-methyl)-piperidin-3-ylmethyl]-N1-(3-methoxy-propyl)-2-(naphthalen-2-ylsulfonylamino-succinamide, MS (ISO): 631.6 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763604 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-835d62137ab141a2a2908702860d134d |
| Source note | uspto-grants-1998_06 |