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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966541Generated: October 30, 2026

Benzaldehyde → N*2*-Benzyl-N*1*-(8-methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine

https://huagongshe.com/reaction/1966541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium borohydrideHCID 4311764—
ReactantN*1*-(8-Methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamineHCID 70276090—
ProductN*2*-Benzyl-N*1*-(8-methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamineHCID 5947481311%

Reaction Conditions

Temperature60 °C

Reaction Steps

N*1*-(8-Methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine (Example 75, 150 mg, 0.488 mmole) and benzaldehyde were stirred at RT for 20 hrs. Molecular sieve (4A) was added and the mixture was heated to 60° C. within 2 hrs. NaBH4 was added and the mixture was stirred for 1 h at RT. The resulting mixture was filtered and extracted with dichloromethane. The organic phases were dried and concentrated. The residue was purified using preparative HPLC (RP-18, water/acetonitrile) to obtain the product (21 mg, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420670B2
Source datasetuspto-grants-2013_04
ORD IDord-27c07801857346188322936edc9b65d5
Source noteuspto-grants-2013_04