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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749030Generated: October 30, 2026

Dimethylamine → HCID 69108521, compound

https://huagongshe.com/reaction/749030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 69230869HCID 69230869—
SolventDichloromethaneHCID 6344—
ProductHCID 69108521HCID 69108521—

Reaction Steps

The hydrogenated compound 60 (2.2 g, 4.96 mmol) was dissolved in CH2Cl2 and stirred at room temperature under an atmosphere of argon. Triethylamine (0.829 mL, 5.95 mmol) and benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent, 2.413 g, 5.456 mmol) were added and the reaction mixture was stirred for 15 min. Dimethylamine (2.0 M solution in THF, 12.4 mL, 24.8 mmol) was added and the resulting solution was stirred at room temperature for about 2-3 h. The solvent was removed under reduced pressure and the resulting oil was taken up in EtOAc (100 mL). The organic layer was extracted with 0.5 N NaOH (1×30 mL), water (2×50.0 mL) and brine (1×50.0 mL). Drying and concentration of the organic layer gave the desired amide crude (1.2 g, ˜98%). Flash chromatography on silica gel (methanol-chloroform 1%-2%) yielded the desired amide 75(0.8 g 98%) 1H NMR (400 MHz, DMSO-d6): 7.32 (dd, J=7.6 and 2 HZ, 1H), 7.21 (m, 3H), 7.08 (dd, J=14 and 7.2 Hz, 2H), 6.83 (d, J=8.8 Hz, 2H), 6.75 (d, J=8.0 Hz, 1H), 4.53 (m, 1H) 3.55 (s, 3H), 2.89 (s, 3H), 2.85-2.58 (m, 7H), 2.59 (t, J=7.6 Hz, 2H), 1.31 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399786B2
Source datasetuspto-grants-2008_07
ORD IDord-4655979183864bd8bd56b35532a7baf4
Source noteuspto-grants-2008_07