HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9387Generated: October 25, 2026
Potassium Carbonate → Tert-butyl [4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamate
https://huagongshe.com/reaction/9387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Tert-butyl [4-(7-bromo-3-nitroquinolin-4-ylamino)butyl]carbamate | HCID 21984414 | — |
| Catalyst | 1,1'-Diethyl-4,4'-bipyridinium dibromide | HCID 11474262 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl [4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamate | HCID 21984174 | 99% |
Reaction Steps
A solution of sodium hydrosulfite (43.35 g, 249 mmol) and potassium carbonate (38.28 g, 277 mmol) in water (300 mL) was added to a mixture of tert-butyl[4-(7-bromo-3-nitroquinolin-4-ylamino)butyl]carbamate (24.3 g, 55.3 mmol) and 1,1′-diethyl-4,4′-bipyridinium dibromide (1.03 g, 2.76 mmol) in dichloromethane (368 mL) and water (40 mL), and the reaction was stirred overnight at ambient temperature. The reaction mixture was filtered through a layer of CELITE filter aid. The aqueous filtrate was extracted with dichloromethane, and the combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 22.4 g of tert-butyl[4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamate as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091214B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ab593658aea3483d87d1ad57cc97e475 |
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| Source note | uspto-grants-2006_08 |
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