HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364021Generated: October 28, 2026
Tetrabutylammonium Fluoride → HCID 58923884, compound
https://huagongshe.com/reaction/1364021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 58923873 | HCID 58923873 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58923884 | HCID 58923884 | 41% |
Reaction Steps
A suspension of 11-{[tert-butyl(dimethyl)silyl]oxy}-9-(methylsulfonyl)-9,10,11,12-tetrahydro-8H-[1,4]diazepino[1′,2′:1,2]imidazo[4,5-c]quinolin-6-amine (1.0 g, 2.2 mmol) in anhydrous THF (30 mL) was cooled to −20° C., and tetrabutylammonium fluoride (2.383 mL of a 1 M solution in THF) was slowly added. The reaction was stirred overnight, and a precipitate formed. The cold reaction mixture was filtered, and the isolated precipitate was washed with THF and dried under high vacuum to provide 313.7 mg of 6-amino-9-(methylsulfonyl)-9,10,11,12-tetrahydro-8H-[1,4]diazepino[1′,2′:1,2]imidazo[4,5-c]quinolin-11-ol as white crystals, mp 282-283° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07888349B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-396b584d85394402830b34d1edbe98f0 |
|---|
| Source note | uspto-grants-2011_02 |
|---|