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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516391Generated: October 30, 2026

Tert-butyl (piperidin-4-ylmethyl)carbamate → HCID 86700765, compound

https://huagongshe.com/reaction/516391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
Reactant1-[4-Chloro-6-(morpholin-4-yl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazoleHCID 53488102—
ProductHCID 86700765HCID 8670076594%

Reaction Steps

Reaction of 1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazole (Example 2) and tert-butyl 4-piperidinylmethylcarbamate as in previous examples gave tert-butyl {1-[4-[2-(difluoromethyl)-4-methoxy-1H-benzimidazol-1-yl]-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-4-piperidinyl}methylcarbamate in 94% yield: mp (CH2Cl2/MeOH) 210-212° C.; 1H NMR (DMSO-d6) δ 7.88 (d, J=8.1 Hz, 1H), 7.68 (t, JHF=52.9 Hz, 1H), 7.40 (t, J=8.2 Hz, 1H), 6.94 (d, J=7.9 Hz, 1H), 6.87 (t, J=5.5 Hz, 1H), 4.68-4.59 (m, 2H), 3.98 (s, 3H), 3.80-3.78 (m, 4H), 3.70-3.69 (m, 4H), 3.05-2.87 (m, 2H), 2.90 (t, J=5.9 Hz, 2H), 1.72 (br, 3H), 1.38 (s, 9H), 1.09 (br, 2H); Anal. Calcd. for C27H36F2N8O4: C, 56.4; H, 6.3; N, 19.5. Found: C, 56.7; H, 6.3; N, 19.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108980B2
Source datasetuspto-grants-2015_08
ORD IDord-cb88208bf0fb4f7493181e395883a2e3
Source noteuspto-grants-2015_08