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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239405Generated: October 29, 2026

1-(Methanesulfonyl)piperidin-4-amine → HCID 57989816, compound

https://huagongshe.com/reaction/239405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methanesulfonyl)piperidin-4-amineHCID 11355826—
ReactantHCID 86636585HCID 86636585—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57989816HCID 5798981684%

Reaction Steps

Following a procedure analogous to the procedure described in Example 1 using N-{5-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (0.30 g, 0.57 mmol), 1-(methylsulfonyl)-4-piperidinamine (0.3 g, 1.7 mmol) and THF (1 mL) the title compound was obtained (0.32 g, 0.48 mmol, 84% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.82 (s, 1H), 8.13 (d, J=5.0 Hz, 1H), 7.71-7.44 (m, 3H), 7.45-7.32 (m, 3H), 7.29 (t, J=9.2 Hz, 1H), 6.30 (m, 1H), 3.50 (m, 2H), 3.30-3.24 (m, 1H), 2.86 (s, 3H), 2.83-2.64 (m, 2H), 1.90 (m, 2H), 1.67-1.44 (m, 2H), 1.36 (d, J=6.8 Hz, 6H). MS (ESI): 667 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642759B2
Source datasetuspto-grants-2014_02
ORD IDord-d3ddcb73d6884c5486512cff1fdb56d8
Source noteuspto-grants-2014_02