HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336876Generated: November 1, 2026
Sodium triacetoxyborohydride → HCID 58525004, compound
https://huagongshe.com/reaction/336876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 58525018 | HCID 58525018 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58525004 | HCID 58525004 | — |
Reaction Steps
To a solution of tert-butyl 4-(4-(6-chloro-3-(hydroxymethyl)quinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperazine-1-carboxylate (400 mg, 0.74 mmol) in dichloromethane(10 mL) at room temperature was added MnO2 (2 g). The resultant solution was stirred for 3 h before filtering through celite and washing with dichloromethane (20 mL). After removal solvent in vacuo, the residue was redisolved in THF (5 mL), to which NaBH(OAc)3 (443 mg, 2.1 mmol) and CH3NH2.HCl (140 mg, 2.1 mmol) were added. The solution was stirred at room temperature overnight, quenched with NaHCO3 (sat. 10 mL), extracted with EtOAc (20 mL×3), and dried over Na2SO4. After removal of solvent in vacuo, the crude product was taken to next step without further purification. LC-MS: (M+H)=550.32
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889706B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-b60ea30bbb7044258620ba2dae618cf3 |
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| Source note | uspto-grants-2014_11 |
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