HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 46213853, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 67378312 | HCID 67378312 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 46213853 | HCID 46213853 | — |
Reaction Steps
A mixture of the crude 1′-(8-chloro-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-1H-spiro[isochromene-4,4′-piperidine] (0.10 g, 0.24 mmol) and paraformaldehyde (0.057 g, 1.9 mmol) in methanol (2 ml) was heated at reflux for 4 h. After cooling to room temperature sodium cyanoborohydride (0.03 g, 0.47 mmol) was added at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 18 h. Quenching with 1 M aqueous sodium hydroxide solution (30 ml) was followed by extraction with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664216B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-34038a108af94c6ca96e3f86d1140ccc |
| Source note | uspto-grants-2014_03 |