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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167064Generated: October 31, 2026

Isobutyraldehyde → HCID 10884258, compound

https://huagongshe.com/reaction/2167064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantTriethylamineHCID 8471—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10905789HCID 10905789—
SolventWaterHCID 962—
ProductHCID 10884258HCID 10884258—

Reaction Steps

To a solution of N4-3-[4(3-aminopropyl)piperazine]propyl-7-chloroquinolin-4-amine (Intermediate of example 12) (150 mg, 0.41 mmol) in CH2C2 (4 mL) isobutyraldehyde (62 μL, 0.46 mmol), triethylamine (26 μL, 0.16 mmol) and 3 Å molecular sieves are added. The reaction media is stirred for 3 h and cooled before NaBH4 (78 mg, 2.05 mmol) is added portionwise over 30 min. Stirring is left for 1.5 h, water (10 mL) is added and the media is filtered. Compound is extracted with CH2Cl2 (3×20 mL). Combined organic layers are dried over MgSO4. Crude compound is purified by thick-layer chromatography (CH2Cl2/MeOH/NH4OH:90/10/1.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09044478B2
Source datasetuspto-grants-2015_06
ORD IDord-2e23454e70cc4b4d97d2c1151f74fa02
Source noteuspto-grants-2015_06