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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641318Generated: November 2, 2026

Diisopropylethylamine → HCID 178457048, compound

https://huagongshe.com/reaction/1641318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58949905HCID 58949905—
ReactantHCID 178517964HCID 178517964—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 178457048HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114887B2
Source datasetuspto-grants-2012_02
ORD IDord-08c10c1b14bf4c27ba94073a3c3b9f98
Source noteuspto-grants-2012_02