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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519174Generated: October 30, 2026

Hydrochloric Acid → HCID 86727582, compound

https://huagongshe.com/reaction/519174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(3S,4S)-4-[(R)-7-(2-fluoro-phenyl)-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl]-3-methyl-piperidine-1-carboxylic acid tert-butyl esterHCID 86727580—
ProductHCID 86727582HCID 8672758253%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of (3S,4S)-4-[(R)-7-(2-fluoro-phenyl)-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl]-3-methyl-piperidine-1-carboxylic acid tert-butyl ester (0.035 g, 0.069 mmol) in HCl (4 M in EtOAc, 10 mL) was stirred at 20° C. for 2 h. The reaction mixture was concentrated in vacuo to give (R)-7-(2-fluoro-phenyl)-4-methyl-6-((3S,4S)-3-methyl-piperidin-4-yl)-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one hydrochloride acid as a colorless solid (0.015 g, 53%). 1H NMR (400 MHz, MeOD) δ 7.52-7.41 (m, 1H), 7.35-7.18 (m, 3H), 6.93 (s, 1H), 6.86 (s, 1H), 4.90 (m, 1H), 4.65 (s, 2H), 3.47 (m, 1H), 3.22-2.94 (m, 4H), 2.84 (d, J=9.8 Hz, 1H), 2.55-2.27 (m, 2H), 2.00-1.80 (m, 3H), 1.51 (d, J=6.4 Hz, 3H), 1.00-0.80 (m, 3H). SFC (Table 1, Method 43), Rt=3.789 min., LC/MS (Table 1, Method 4) Rt=1.748 min.; MS m/z: 409 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-1f27b9ebfd414b31a07c536dd897ab3d
Source noteuspto-grants-2015_08