HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81094Generated: October 28, 2026
Sodium triacetoxyborohydride → HCID 178452762, compound
https://huagongshe.com/reaction/81094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Tert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamate | HCID 86724467 | — |
| Reactant | HCID 178461263 | HCID 178461263 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178452762 | HCID 178452762 | — |
Reaction Steps
To a solution of tert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamate (353 g, 1.27 mol) and trans-4-methylcyclohexanecarbaldehyde (160 g, 1.27 mol) in DCM (8.0 L) and acetic acid (2 ml) was added sodium triacetoxyborohydride (807.7 g, 3.81 mol) at 0° C. The mixture was stirred for 15 min, and then warmed to room temperature. The mixture was stirred for 15 h at room temperature and then quenched with water (10 L). The mixture was filtered, the filtrate was separated, and the organic layer was concentrated under reduced pressure to give crude product. The crude product was purified over a silica gel column, eluting with EtOAc: petroleum ether (0-1:10), to give tert-butyl (2,6-dichloro-3-(((trans-4-methylcyclohexyl)methyl)amino)pyridin-4-yl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846657B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-2e2147643ee740edbd6d3d744142f8be |
|---|
| Source note | uspto-grants-2014_09 |
|---|