HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 24989849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 24989848 | HCID 24989848 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 24989849 | HCID 24989849 | — |
Reaction Steps
5-Chloro-N-((1-(4-(2-oxopiperazin-1-yl)phenyl)-1H-1,2,3-triazol-4-yl)methyl)thiophene-2-carboxamide (24 mg, 0.06 mmol, prepared as shown in Example 60) was stirred in 2 mL acetic acid at RT. To it was added formaldehyde (37% in water, 22 μL, 0.3 mmol). The mixture was stirred for 10 min. NaBH3CN (30 mg, 0.48 mmol) was added. The reaction was allowed for 10 min, and directly subjected to reverse phase prep HPLC to isolate the title compound. MS found for C19H19ClN6O2S (M+H)+ 431.1, 433.1 (Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696352B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-2854cf15101c41e3ab8e0e5fc8ddd51f |
| Source note | uspto-grants-2010_04 |