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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525332Generated: October 27, 2026

Diisopropylethylamine → HCID 178457728, compound

https://huagongshe.com/reaction/1525332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-(4-Bromophenyl)propan-2-amineHCID 23009116—
ReactantHCID 178524753HCID 178524753—
SolventDimethylformamideHCID 6228—
ProductHCID 178457728HCID 17845772857%

Reaction Steps

A mixture of 4-hydroxy-2-(pyridazin-3-yl)pyrimidine-5-carboxylic acid, 30-ie, (110 mg, 0.5 mmol), 2-(4-bromophenyl)propan-2-amine, 36-b, (70 mg, 0.32 mmol), HATU (290 mg, 0.76 mmol) and DIEA (82 mg, 0.64 mmol) in DMF (3 mL) was stirred at room temperature overnight. The mixture was washed with aqueous NH4Cl (15 mL) and extracted with EtOAc (30 mL). The organic layers were dried and concentrated in vacuo. The residue was washed with hexane to afford compound 36-c (80 mg, 57%). 1H NMR (300 MHz, CDCl3) δ11.62 (s, 1H), 9.55 (s, 1H), 9.41 (dd, J=1.5, 4.8 Hz, 1H), 9.00 (d, J=4.2 Hz, 1H), 8.63 (dd, J=1.5, 8.1 Hz, 1H), 7.78 (dd, J=5.1, 8.4 Hz, 1H)), 7.43 (d, J=8.4 Hz, 2H), 7.33 (d, J=8.4 Hz, 2H), 1.78 (s, 6H). LC-MS: (M+H)+ 414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079930B2
Source datasetuspto-grants-2015_07
ORD IDord-df12f5bd23954d7ea4c273276289ed87
Source noteuspto-grants-2015_07