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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112149Generated: October 31, 2026

2-(Aminomethyl)aniline → HCID 67411378, compound

https://huagongshe.com/reaction/2112149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Aminomethyl)anilineHCID 178096—
Reactant3-tert-Butyl-1-methyl-1H-pyrazol-5-amineHCID 2735287—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67411378HCID 6741137849.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

5-tert-Butyl-2-methyl-2H-pyrazol-3-ylamine (10s) (4.8 g, 31 mmol) and carbonyl diimidazole (4.6 g, 32 mmol) were partially dissolved in DCE (100 mL) and heated at 70° C. for 2 hours. The reaction was cooled and 2-aminomethyl-phenylamine (9s) (4.2 g, 34 mmol) was added and the reaction was stirred 14 hours. The reaction was concentrated to remove the solvent and then partitioned between EtOAc and 0.5N HCl (60 mL). The organic phase was washed with NH4Cl and water and dried (MgSO4). The solution was concentrated and recrystallized from EtOAc (200 mL) to provide the desired product (5s) (4.6 g, 49% yield). 1H NMR (400 MHz, DMSO-d6) δ 8.31 (s, 1H), 6.98 (d, J=1.6 Hz, 1H), 6.96 (dt, J=7.8, 1.6 Hz, 1H), 6.63 (t, J=6.3 Hz, 1H), 6.59 (d, J=7.0 Hz, 1H), 6.48 (t, J=6.3 Hz, 1H), 5.93 (s, 1H), 5.07 (s, 2H), 4.12 (d, J=6.3 Hz, 2H), 3.51 (s, 3H), 1.16 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521447B2
Source datasetuspto-grants-2009_04
ORD IDord-a35ff4dd0f8149f388a6c29820e655b3
Source noteuspto-grants-2009_04