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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575163Generated: October 31, 2026

4-Aminomethyltetrahydropyran → HCID 71715228, compound

https://huagongshe.com/reaction/575163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminomethyltetrahydropyranHCID 2773210—
Reactant2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acidHCID 86693171—
ProductHCID 71715228HCID 71715228—

Reaction Steps

2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acid (0.05 g) was reacted with 1-tetrahydro-2H-pyran-4-ylmethanamine similar to as described in Example 2 to afford 6 mg of 9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-N3-(tetrahydropyran-4-ylmethyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2,3-dicarboxamide following reverse phase hplc purification. MS (Q1) 471 (M)+. NMR (400 MHz, DMSO) δ 11.30 (t, J=5.4 Hz, 1H), 8.60 (d, J=8.4 Hz, 1H), 8.38 (s, 1H), 7.89 (s, 1H), 7.01 (d, J=10.6 Hz, 1H), 5.47 (s, 1H), 5.05-4.97 (m, 2H), 4.59-4.51 (m, 2H), 3.91-3.74 (m, 3H), 3.19 (t, J=6.0 Hz, 2H), 1.82-1.67 (m, 1H), 1.67-1.58 (m, 2H), 1.49 (s, 6H), 1.32-1.18 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-b4c3c5dc194b437db95fc733f7390285
Source noteuspto-grants-2015_05