Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18771820 | HCID 18771820 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18772120 | HCID 18772120 | — |
Reaction Steps
To a suspension of N-[2-(4-pyridinyl)-4-thiazolyl]-N′-2-[6-(piperidon-4-yl)methyl]urea (50 mg, 0.12 mmol, Example 175) in MeOH (10 mL) was added propylamine (0.1 mL, 1.22 mmol). The resulting mixture was heated at 50° C. for 4 h under N2. After the mixture was cooled to RT, NaBH4 (83 mg, 2.20 mmol) was added. The mixture was stirred at RT under N2 for 3 h. Solvent was removed in vacuo and the crude product was purified by chromatography on silica gel. Elution with CH2Cl2:MeOH (90:10) gave the title compound as a white solid. MS m/z: 451.7 (M+H). Calc'd. for C23H29N7OS-451.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07196104B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-3c2b6c861117487887ae980848ba20b8 |
|---|
| Source note | uspto-grants-2007_03 |
|---|