Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 178491363 | HCID 178491363 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178491359 | HCID 178491359 | — |
Reaction Steps
A mixture of 100 mg (0.25 mmol) N-(2,6-dimethoxybenzyl)-N′-(4-pyrrolidine-2-yl-1,3-thiazole-2-yl)guanidine hydrochloride, Example 147, 0.021 ml acetyl chloride and 0.04 ml pyridine in 10 ml THF were stirred for 1 hour at 5° C. and then 4 hours at room temperature. Chromatography of the crude product on RP-silica gel (Chromabond column, acetonitrile/water+0.1% glacial acetic acid; 0-100%) yielded 33 mg of the desired product; ESI-MS [M+H+]=404.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481576B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8a9d1ad6439a491eb54df1e74434a6e0 |
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| Source note | uspto-grants-2013_07 |
|---|