HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641318Generated: November 2, 2026
Diisopropylethylamine → HCID 178457048, compound
https://huagongshe.com/reaction/1641318
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 58949905 | HCID 58949905 | — |
| Reactant | HCID 178517964 | HCID 178517964 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 178457048 | HCID 178457048 | — |
Reaction Steps
To a 20 mL dichloroethane solution of 0.35 g (0.92 mmol) 4-(cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-one and 0.25 mL (1.4 mmol) DIEA went 0.16 g (0.92 mmol) 3-(3-formylphenyl)-2-methylpropanenitrile (9-3). The suspension was allowed to stir for 10 min then 0.4 g (1.9 mmol) sodium triacetoxyborohydride was added and the reaction was allowed to stir at rt overnight. HPLC/MS showed no starting material so the reaction was quenched with 100 mL sat NaHCO3 and diluted with CH2Cl2. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The remaining oil was purified on an Isco automated system affixed with a Biotage Flash 25(M) cartridge eluted with 5% MeOH+0.5M NH3 in CH2Cl2 at 25 mL/min over 30 min. The product eluted second.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114887B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-08c10c1b14bf4c27ba94073a3c3b9f98 |
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| Source note | uspto-grants-2012_02 |
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