Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968163Generated: October 30, 2026

Diisopropylethylamine → 4-(3-amino-2,2-difluoropropylamino)-4-methyl-1-(2-nitro-1H-imidazol-1-yl)-3-pentanone oxime

https://huagongshe.com/reaction/968163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-chloro-4-methyl-1-(2-nitro-1H-imidazol-1-yl)-3-nitrosopentaneHCID 15185994—
Reactant2,2-Difluoropropane-1,3-diamine dihydrochlorideHCID 22287769—
SolventAcetonitrileHCID 6342—
Product4-(3-amino-2,2-difluoropropylamino)-4-methyl-1-(2-nitro-1H-imidazol-1-yl)-3-pentanone oximeHCID 73880184—

Reaction Steps

To a mixture of 1,3-diamino-2,2-difluoropropane dihydrochloride (title A diamine) (1.10 g, 6.01 mmol) and N,N-diisopropylethylamine (2.72 g, 21.04 mmol) in acetonitrile (10 mL) at 40° C. was added 4-chloro-4-methyl-1-(2-nitro-1H-imidazol-1-yl)-3-nitrosopentane (Example 3, step (B)) (0.50 g, 1.90 mmol) in small portions with stirring under nitrogen atmosphere. After the addition, the stirring was continued for an additional 30 minutes and the solvent was removed on a rotary evaporator. The paste obtained was treated with silica gel and the silica gel powder impregnated with the compound was loaded onto a silica gel column and eluted with CH3OH—CH2Cl2 (5:95). The fractions containing compound were collected and evaporated to give the title product as a light yellow colored solid. Yield: 0.42 g (66%), mp. 112-114° C.; 1H NMR (CDCl3) d 1.19 [s, 6H, C(CH3)2], 2.88 [m, 4H, C(═N)CH2 & NHCH2], 3.71 (t, 3H, JHF=13.19 Hz, CH2NH2), 4.72 (t, 2H, J=7.26, CH2CH2N), 7.11 & 7.26 (2s, 2H, nitroimid-H) and 10.79 (s, 1H, NOH). MS m/e 335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958141B2
Source datasetuspto-grants-2005_10
ORD IDord-be0d93a345e34cafae3cd392cb69fec6
Source noteuspto-grants-2005_10