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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622936Generated: October 31, 2026

HCID 77150664, compound → HCID 76182140, compound

https://huagongshe.com/reaction/1622936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 77150664HCID 77150664—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 76182140HCID 7618214057%

Reaction Steps

racemic-(3S,4aR,6aR,14aS)—N-[(2,4-Difluorophenyl)methyl]-11,13-dioxo-3-phenyl-12-[(phenylmethyl)oxy]-1,3,4,4a,5,6a,7,11,13,14a-decahydro-2H-pyrido[1′,2′:4,5]pyrazino[1,2-a][3,1]benzoxazine-10-carboxamide (27 mg, 0.0432 mmol) was suspended in methanol, 10 w.t, % Pd/C (3 mg) was added and hydrogen was bubbled through the system several times until the reaction was determined complete by TLC (5% methanol/dichloromethane). The suspension was filtered through Celite eluting with methanol/chloroform and the filtrate was concentrated under reduced pressure and purified by HPLC to give the title compound (13 mg, 57%) as a white solid, 1H NMR (CDCl3) δ 12.40 (br s, 1H), 10.37 (m, 1H), 8.32 (s, 1H), 7.37-7.28 (m, 3H), 7.24-7.15 (m, 4H), 6.79 (m, 2H), 5.78 (br s, 1H), 4.85 (m, 1H), 4.62 (m, 2H), 4.29 (m, 1H), 4.16-4.09 (m, 2H), 3.92 (dd, J=11.6, 4.8 Hz, 1H), 2.58 (m, 1H), 2.46 (m, 1H), 2.07-1.64 (m, 7H); ES+ MS: 536 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778943B2
Source datasetuspto-grants-2014_07
ORD IDord-9b04fa1febba4082a732fad8fe61e23a
Source noteuspto-grants-2014_07