HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 67188838, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67188470 | HCID 67188470 | — |
| Product | HCID 67188838 | HCID 67188838 | — |
Reaction Steps
A solution of tert-butyl 4-(4-bromo-2-cyanophenylamino)piperidine-1-carboxylate (1.00 g, 3 mmol) in THF (10 ml, 123 mmol) under argon was added borane-tetrahydrofuran complex (8 ml, 8 mmol) and stirred at RT for 20 h. The reaction was cooled to 0° C. and quenched with MeOH. The mixture was further diluted with EtOAc and washed with saturated aqueous NaHCO3 and brine, then dried (MgSO4). Evaporation gave a relatively pure crop of the desired product, tert-butyl 4-(2-(aminomethyl)-4-bromophenylamino)piperidine-1-carboxylate, which was used directly in the next step without further purification. MS m/e 385.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935709B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-b0f2decdd279429a84e6ad0661a71423 |
| Source note | uspto-grants-2011_05 |