HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14606675, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Amino-4,6-dichloropyrimidine | HCID 79434 | — |
| Reactant | HCID 14606672 | HCID 14606672 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14606675 | HCID 14606675 | 58% |
Reaction Steps
To a 50 mL round bottom flask fitted with a reflux condenser was added (2R-cis)-4-aminotetrahydro-2-furanmethanol, Compound IV(f), (184 mg, 1.57 mmole), 5-amino-4,6-dichloro-pyrimidine (770 mg, 4.70 mmole), triethylamine (0.44 mL, 3.16 mmole) and t-butyl alcohol (16 mL). The reaction mixture was heated to reflux temperature under an atmosphere of argon for 72 hours, at which time the volatile materials were removed by rotary evaporation. The residue was dissolved in 100 mL EtOAc, washed with saturated NaHCO3 solution (50 mL) and saturated NaCL solution (50 mL), then dried over MgSO4. After filtration and evaporation, the product was purified by flash column chromatography (50% EtOAc/50% Hexane) to yield 220 mg (58%) of Compound IX.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05126347 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-893ec9ab4eb441ce9754fa0c414363f5 |
| Source note | uspto-grants-1992_06 |