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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390347Generated: October 31, 2026

Hexachloroethane → HCID 58458920, compound

https://huagongshe.com/reaction/390347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67115353HCID 67115353—
SolventAcetonitrileHCID 6342—
ProductHCID 58458920HCID 5845892097.3%

Reaction Steps

To stirred solution of 3-(benzyloxy)-N′-(2-(4-fluorophenyl)acetyl)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carbohydrazide (0.075 g, 0.16 mmol), Ph3P (0.074 g, 0.28 mmol) and DIEA (0.16 mL, 0.91 mmol) in anhydrous CH3CN (3 mL) was added hexachloroethane (0.048 g, 0.20 mmol) all at once at room temperature. After 4 h, the resulting greenish-yellow reaction mixture was purified by preparative HPLC on a C18 column using water/MeOH containing 0.1% TFA as eluent to afford title compound (0.072 g, 86% yield) as a yellow solid. 1HNMR (500 MHz, CDCl3) δ: 7.42-7.40 (2H, m), 7.30-7.28 (3H, m), 7.24 (2H, dd, J=8.2, 5.55.34 (2H, s), 4.20 (2H, s), 4.07-4.01 (4H, m), 1.64 (6H, s). Hz)), 6.99 (2H, t, J=8.6 Hz), HRMS (M+H) calcd for C25H24N4O4F: 463.1782. found: 463.1788.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383639B2
Source datasetuspto-grants-2013_02
ORD IDord-7efcb5f0677f4469aac92af4753aca87
Source noteuspto-grants-2013_02