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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525723Generated: October 27, 2026

tert-Butyl 4,7-diazaspiro(2.5)octane-4-carboxylate → HCID 118045016, compound

https://huagongshe.com/reaction/525723

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4,7-diazaspiro(2.5)octane-4-carboxylateHCID 51358567—
Reactant6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamideHCID 86702637—
ProductHCID 118045016HCID 118045016—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Example 33 using 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamide (Stage 48.2) and tert-butyl 4,7-diazaspiro[2.5]octane-4-carboxylate to afford an off-white powder. HPLC (Condition 4) tR=4.44 min, UPLC-MS (Condition 3) tR=0.81 min, m/z=475 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 0.27-0.54 (m, 4H) 2.82 (br. s, 2H) 2.96-3.20 (m, 5H) 6.64 (br. s, 1H) 7.32 (d, J=8.21 Hz, 2H) 7.86 (d, J=8.99 Hz, 3H) 8.29 (br. s, 1H) 8.71 (br. s, 1H) 10.37 (br. s, 1H) 13.00 (br. s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340537B2
Source datasetuspto-grants-2016_05
ORD IDord-c6706a0cf2c045a2a459fe1fc0f079ff
Source noteuspto-grants-2016_05