HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67391050, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| Reactant | 6-Bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chloride | HCID 57439900 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67391050 | HCID 67391050 | 72.8% |
Reaction Steps
To a solution of tert-butyl 1,4-diazepane-1-carboxylate (0.621 g) and triethylamine (0.864 mL) in THF (12 mL) was added dropwise a solution of 6-bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chloride (Example 46a, 1 g) in THF (20 mL). The reaction was stirred at room temperature for 20 min. The resulting solution was concentrated under reduced pressure, acidified with 2 M HCl, and extracted into ethyl acetate. The combined organics were dried (MgSO4), filtered and evaporated under reduced pressure to give the subtitle compound (1.097 g) that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012980B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-d40b05ca164147fabfb0fb1ea4d392dc |
| Source note | uspto-grants-2011_09 |