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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426983Generated: November 2, 2026

Diisopropylethylamine → HCID 59232897, compound

https://huagongshe.com/reaction/2426983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 783440HCID 783440—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 59232611HCID 59232611—
SolventAcetonitrileHCID 6342—
ProductHCID 59232897HCID 5923289758%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of the acid of Preparation 14a (51 mg, 0.142 mmol) in CH3CN (3 mL) were added 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC) (48.3 mg, 0.213 mmol) and 1-hydroxy-7-benzotriazole (HOBt) (34 mg, 0.213 mmol). After stirring for 5 minutes, to the solution were added 4-(4-methyl-naphthalen-1-yl)-thiazol-2-ylamine (50.4 mg, 0.426 mmol) and diisopropylethyl amine (0.742 ml, 0.426 mmol). The reaction was heated at 75° C. for 12 hours. The reaction mixture was filtered, and purified by preparative HPLC to give the title compound of Example 222 as a white solid (36 mg, 58% yield). LC/MS (m/z) 440.17 [(M+H)+]; HPLC Rt: 3.12 min. 1H NMR (400 MHz, CDCl3): δ 7.34 (1H, m), 7.18-7.26 (5H, m), 6.79-6.93 (4H, m), 4.42 (1H, s), 3.78 (4H, m), 3.06 (4H, m), 1.34 (6H, s). LC/MS (m/z) 440.17 [(M+H)+]; HPLC Rt: 3.120 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968577B2
Source datasetuspto-grants-2011_06
ORD IDord-3f3ab3ba2a2a4b939ebfb89e6544bba9
Source noteuspto-grants-2011_06