HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532919Generated: October 31, 2026
HCID 86711365, compound → HCID 73335824, compound
https://huagongshe.com/reaction/532919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86711365 | HCID 86711365 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 73335824 | HCID 73335824 | 31.9% |
Reaction Steps
To a degassed solution of 9-iodo-2-(4-isopropyl-1H-imidazol-1-yl)-7,8-dihydro-[1,4]diazepino[7,1-a]isoquinolin-5(4H)-one (20 mg, 0.045 mmol) and PdCl2(dppf)-CH2Cl2 adduct (2 mg, 2.24 μmol) in dioxane (1 mL) was added diethylzinc (135 μL, 0.135 mmol, 1M in hexane) and the mixture was heated in the microwave at 80° C. for 44 h. The reaction mixture was allowed to warm to rt and then diluted with AcOEt and 2M aqueous HCl. The organic phase was separated, dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by SFC (column: Diol 5 μm, 250×30 mm, 60A, Princeton; eluent: 7% MeOH/CO2 for 1 min, then from 7% MeOH/CO2 to 12% MeOH/CO2 in 6 min; flow 100 mL/min; UV detection at 220 nm) to yield the title compound (5 mg). UPLC-MS: MS 349.2 (M+H+); UPLC rt 1.01 min. 1H NMR (400 MHz, CHLOROFORM-d): δ ppm 1.21-1.28 (m, 9H) 2.72 (q, J=7.4 Hz, 2 H) 2.85-2.92 (m, 1 H) 2.96 (t, J=6.2 Hz, 2 H) 3.91 (t, J=6.3 Hz, 2 H) 4.35 (br. s., 2 H) 6.61 (s, 1 H) 7.18 (s, 1 H) 7.27-7.38 (m, 2 H) 7.52 (d, J=7.3 Hz, 1 H) 7.93 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08853203B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-fee8da637c0744009c3654931bfcd78a |
|---|
| Source note | uspto-grants-2014_10 |
|---|