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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516342Generated: October 29, 2026

Methanesulfonyl chloride → HCID 46917804, compound

https://huagongshe.com/reaction/516342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67546103HCID 67546103—
ProductHCID 46917804HCID 4691780490%

Reaction Steps

Reaction of the above amine with methanesulfonyl chloride as in Example 21 gave N1-[4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-N3,N3-dimethyl-N1-[1-(methylsulfonyl)-4-piperidinyl]-1,3-propanediamine in 90% yield. Hydrochloride: 1H NMR (DMSO-d6) (rotamers) δ 10.17 and 10.0 (2br, 1H), 8.36 and 8.34 (2d, J=7.0 and 7.9 Hz, 1H), 7.76 and 7.74 (2t, JHF=52.8 Hz, 1H), 7.86 (d, J=8.3 Hz, 1H), 7.57-7.53 (m, 1H), 7.46-7.43 (m, 1H), 4.70-4.56 (m, 1H), 3.84-3.71 (m, 10H), 3.62-3.53 (m, 2H), 3.13-3.06 (m, 2H), 2.94 and 2.93 (2s, 3H), 2.90-2.80 (m, 2H), 2.74 and 2.70 (2s, 6H), 1.99-1.87 (m, 6H); Anal. Calcd. for C26H38ClF2N9O3S.0.5H2O: C, 48.9; H, 6.15; N, 19.7; Cl, 5.6. Found: C, 48.9; H, 6.3; N, 19.8; Cl, 5.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108980B2
Source datasetuspto-grants-2015_08
ORD IDord-2d4b55d63c3248308072bf72a8e7d041
Source noteuspto-grants-2015_08