HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926293Generated: October 25, 2026
HCID 86711379, compound → 9-Propyl-3,4,7,8-tetrahydro-[1,4]diazepino[7,1-a]isoquinoline-2,5-dione
https://huagongshe.com/reaction/926293
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86711379 | HCID 86711379 | — |
| Reactant | HCID 178455869 | HCID 178455869 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 9-Propyl-3,4,7,8-tetrahydro-[1,4]diazepino[7,1-a]isoquinoline-2,5-dione | HCID 89980680 | — |
Reaction Steps
90-1. To a degassed solution of 9-iodo-3,4,7,8-tetrahydro-[1,4]diazepino[7,1-a]isoquinoline-2,5-dione (1.0 g, 2.82 mmol) and propylzinc(II)-bromide (14.1 mL, 7.05 mmol, 0.5M in THF) in dioxane (28 mL) was added PEPPSI-iPr (0.29 g, 0.424 mmol) under argon and the mixture was heated in a pressure vessel at 120° C. for 2.5 h. The reaction mixture was allowed to warm to rt and the solvent was removed under reduced pressure. The residue was suspended in DCM/MeOH (9:1, v/v), filtrated through a pad of celite and the filtrate was evaporated under reduced pressure. The crude product was purified by flash-column chromatography over silicagel (Biotage Isolera Four, eluent: from 1% MeOH in DCM to 10% MeOH in DCM in 35 min) to yield the product as an oil. The title compound was crystallized from diethyl ether to afford yellow crystals (370 mg). UPLC-MS: MS 271.2 (M+H+); UPLC rt 0.86 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284331B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-fcfe984a7f034b21b99a57463aa20f44 |
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| Source note | uspto-grants-2016_03 |
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