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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397265Generated: October 30, 2026

(4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methanamine → HCID 67324310, compound

https://huagongshe.com/reaction/1397265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methanamineHCID 67322930—
ReactantHCID 67325171HCID 67325171—
ProductHCID 67324310HCID 6732431045%

Reaction Steps

This compound was synthesized from (4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methanamine and 3-ethyl-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described in example 8 step 6 (85 mg, yield 45%). 1H NMR (400 MHz, CDCl3) δ 8.29 (s, 1H), 8.05 (s, 1H), 7.89 (m, 2H), 7.80 (s, 1H), 7.52 (m, 2H), 7.37-7.29 (m, 3H), 4.00-3.94 (m, 2H), 3.89 (d, J=5.5 Hz, 2H), 3.78-3.72 (ddd, J=11.7 Hz, 7.8 Hz, 3.3 Hz, 2H), 2.69 (q, J=7.7 Hz, 2H), 2.36-2.30 (ddd, J=13.6 Hz, 6.5 Hz, 3.3 Hz, 2H), 2.08-2.02 (ddd, J=13.6 Hz, 7.7 Hz, 3.3 Hz, 2H), 1.23 (t, J=7.7 Hz, 3H). MS (ESI) m/z: Calculated for C27H25F3N4O3S: 542.16. found: 543.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-842c1600401f41758a0e8435f382bee7
Source noteuspto-grants-2014_12