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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874310Generated: October 30, 2026

1,2-Dichloroethane → HCID 86671992, compound

https://huagongshe.com/reaction/874310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
ReactantHCID 86671991HCID 86671991—
SolventDichloromethaneHCID 6344—
ProductHCID 86671992HCID 8667199245.7%

Reaction Steps

A suspension of (±)-(E)-3-{1′-benzyl-3,4-dihydro-4-oxo-spiro[2H-(1,3)-benzoxazine-2,3′-piperidin]-6-yl}-acrylic acid (230 mg, 0.55 mmol) in DCM (6 ml) was treated with TEA (0.12 ml, 0.90 mmol) and then with EDC (172 mg, 0.900 mmol), HOBt (121 mg, 0.896 mmol) and NH2OTHP (84 mg, 0.72 mmol) following the procedure described in Example 30, Step B, giving (±)-(E)-3-{1′-benzyl-3,4-dihydro-4-oxo-spiro[2H-(1,3)-benzoxazine-2,3′-piperidin]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide (120 mg) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980877B2
Source datasetuspto-grants-2015_03
ORD IDord-cfdeaf57f111447e9271bc6de9e36c9b
Source noteuspto-grants-2015_03