HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tris(hydroxymethyl)aminomethane → HCID 22137332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride | HCID 2736421 | — |
| Reactant | [4-(2-Pyrrolidin-1-yl-ethoxy)-phenyl]-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-amine | HCID 22137433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22137332 | HCID 22137332 | 101% |
Reaction Steps
To a solution of [4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-amine (0.060 g, 0.15 mmol) in 0.4 mL methylene chloride was added triethylamine (0.06 mL, 0.45 mmol) and 4-bromo-2-trifluoromethoxybenzenesulfonyl chloride (0.103 g, 0.3 mmol). The reaction mixture was stirred at room temperature for 24 hr. PS-isocyanate resin (0.050 g) and PS-trisamine resin (0.050 g) were added and the reaction mixture was stirred for 2 hr. at room temperature. The resin was filtered off with the aid of methylene chloride. The filtrate was concentrated to afford the title compound of Step A (0.106 g). MS 700.8 (M+1)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053212B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-2834787f09ad4bec8564df820a33f084 |
| Source note | uspto-grants-2006_05 |