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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516287Generated: October 30, 2026

2,4-Dichloro-6-morpholino-1,3,5-triazine → HCID 86645851, compound

https://huagongshe.com/reaction/516287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-morpholino-1,3,5-triazineHCID 81076—
ReactantHCID 23082131HCID 23082131—
SolventAcetoneHCID 180—
ProductHCID 86645851HCID 86645851—

Reaction Steps

Reaction of 4-(tert-butyldimethylsilyloxy)-2-(difluoromethyl)-1H-benzimidazole with 2,4-dichloro-6-(4-morpholinyl)-1,3,5-triazine as in Example 2, but using acetone as solvent, followed by chromatography on silica gel eluting with CH2Cl2/hexanes 3:1 gave 4-(tert-butyldimethylsilyloxy)-1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-1H-benzimidazole: mp (hexanes) 143-145° C.; 1H NMR (CDCl3) δ 7.99 (d, J=8.4 Hz, 1H), 7.46 (t, JHF=53.5 Hz, 1H), 7.32 (t, J=8.2 Hz, 1H), 6.88 (d, J=8.0 Hz, 1H), 3.96 (m, 3.5H), 3.88 (m, 0.5H), 3.81 (m, 3.5H), 3.75 (m, 0.5H), 1.05 (s, 9H), 0.29 (s, 6H); MS (APCI+) 497.9/499.9 MH+. Anal. Calcd. for C21H27ClF2N6O2Si: C, 50.75; H, 5.5; N, 16.9. Found: C, 50.7; H, 5.6; N, 17.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108980B2
Source datasetuspto-grants-2015_08
ORD IDord-ce8aba044d2a40b0a382a7bea6c9245d
Source noteuspto-grants-2015_08