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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619796Generated: November 1, 2026

Diisopropylethylamine → HCID 67545781, compound

https://huagongshe.com/reaction/1619796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[4-Chloro-6-(morpholin-4-yl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazoleHCID 53488102—
ReactantHCID 61637468HCID 61637468—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67545781HCID 6754578190%

Reaction Steps

A mixture of tert-butyl 3-[(3-hydroxypropyl)amino]-1-piperidinecarboxylate (516 mg, 2.00 mmol), 1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazole (610 mg, 1.54 mmol), and DIPEA (1.5 mL, excess) in DMF (20 mL) was stirred at room temperature for 2 days. The reaction mixture was diluted with water and extracted with CH2Cl2 (3×30 mL). The combined extracts were washed with water, dried over Na2SO4, and concentrated. Chromatography of the residue on SiO2 eluting with a gradient of CH2Cl2/EtOAc (0-40%) gave tert-butyl 3-[[4-[2-(difluoromethyl)-4-methoxy-1H-benzimidazol-1-yl]-6-(4-morpholinyl)-1,3,5-triazin-2-yl](3-hydroxypropyl)-amino]-1-piperidinecarboxylate (854 mg, 90%): mp (CH2Cl2/hexanes) 109-191° C.; 1H NMR (DMSO-d6) (rotamers) δ 8.00 and 7.88 (2d, J=8.3, 8.4 Hz, 1H), 7.79 and 7.63 (2t, JHF=53.0 Hz, 1H), 7.40-7.33 (m, 1H), 6.94 (dd, J=8.0, 4.13 Hz, 1H), 4.60-4.48 and 4.29 (m, 2H), 3.98 and 3.97 (2s, 3H), 3.97-3.48 (m, 16H), 2.93-2.88 and 2.66-2.64 (2 m, 2H), 1.99-1.69 (m, 3H), 1.52-1.17 (m, 10H); Anal. Calcd. for C29H40F2N8O5: C, 56.3; H, 6.5; N, 18.1. Found: C, 56.4; H, 6.4; N, 18.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772287B2
Source datasetuspto-grants-2014_07
ORD IDord-8d1b75ab297a492d91bf76a4046652a6
Source noteuspto-grants-2014_07