HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 57741270, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 86605022 | HCID 86605022 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57741270 | HCID 57741270 | — |
Reaction Steps
A solution of 0.3 g (0.85 mmol)) 4-(7-acetylamino-4,5-dihydro-pyrazolo[3′,4′:3,4]benzo[1,2-d]thiazol-1-yl)-benzoic acid (prepared analogously to Example 1), 0.32 g (1.00 mmol) TBTU and 0.75 ml (4.38 mmol) diisopropylethylamine in 25 ml dichloromethane is stirred for 15 minutes at ambient temperature and then combined with 0.17 g (0.86 mmol) 4-N-Boc-aminopiperidine. After 2.5 hours the reaction mixture is poured onto 25 ml 5% potassium carbonate solution. The organic phase is dried and evaporated down. The residue is triturated with ethyl acetate/ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232286B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-d05d2ff7e8de4f469225a4dc9b70176d |
| Source note | uspto-grants-2012_07 |