HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383155Generated: October 30, 2026
Isopropanol → Tert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate
https://huagongshe.com/reaction/2383155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | HCID 69027554 | HCID 69027554 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate | HCID 68900070 | 108.8% |
Reaction Steps
tert-Butyl[4-(7-benzyloxy-3-nitroquinolin-4-ylamino)butyl]carbamate (20.36 g, 43.6 mmol) was slurried in toluene (450 mL) and added to a Parr vessel charged with 5% platinum on carbon (4.3 g) and a small amount of toluene. 2-Propanol (50 mL) was added, and the vessel was charged with hydrogen (30 psi, 2.1×105 Pa). The hydrogen was replaced three times. After 4 hours, the catalyst was removed by filtration through a layer of CELITE filter aid, and the filter cake was rinsed with toluene (0.5 L), 50% toluene/2-propanol (0.5 L), and 2-propanol (0.25 L). The filtrate was concentrated under reduced pressure, and the residue was mixed with toluene and concentrated under reduced pressure to provide 20.7 g of tert-butyl[4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate as a viscous, black oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263594B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-2b3e91a1fdf3469bb1b094e4bc978ba3 |
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| Source note | uspto-grants-2012_09 |
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