HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[6-(2,2,2-Trifluoro-acetylamino)-hexanoylamino]-benzenesulfonyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobenzenesulfonyl azide | HCID 11206408 | — |
| Reactant | 6-(Trifluoroacetamido)hexanoyl chloride | HCID 11436518 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[6-(2,2,2-Trifluoro-acetylamino)-hexanoylamino]-benzenesulfonyl azide | HCID 86626124 | — |
Reaction Steps
To 0.57 g (3 mmol) of para-amino-benzenesulfonyl azide dissolved in 5 mL dimethylformamide was added 0.9 mL (6 mmol) triethylamine, then the (2,2,2-trifluro-acetylamino)-hexanoyl chloride dissolved in 10 mL dimethylformamide was added dropwise. The mixture turned brown and was stirred under argon for 24 hrs. Solvent was evaporated, and the remaining oil was dissolved in 10 mL dichloromethane and left at room temperature for 1 hr. The precipitate was filtrated and the solution was evaporated to yield 1.10 g crude oil. The obtained compound was directly used in oligonucleotide synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795423B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-223c7ad2ab5a4003b0395fa342dfae5c |
| Source note | uspto-grants-2010_09 |