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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908665Generated: October 31, 2026

Morpholine → HCID 67394150, compound

https://huagongshe.com/reaction/908665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
Reactant5-Methoxy-4-nitro-1,3-benzothiazole-2-carboxylic acidHCID 45480359—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductHCID 67394150HCID 6739415033%

Reaction Steps

980 mg (2.1 mmol; 1.1 eq.) of bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBroP) is added to 500 mg (1.97 mmol) of 5-methoxy-4-nitro-1,3-benzothiazole-2-carboxylic acid and 344 μl (1.97 mmol; 1 eq.) of diisopropylethylamine in solution in 40 ml of dichloromethane. The reaction mixture is maintained for 15 minutes under stirring at ambient temperature, then 202 μl (2.3 mmol; 1.2 eq.) of morpholine and a spatula tip's worth of dimethylaminopyridine are added to the medium which is maintained under stirring for 18 hours at ambient temperature. An insoluble part is then filtered and the solvent evaporated off under reduced pressure. The residue is then purified on a silica column (eluent: ethyl acetate/heptane: gradient of 30 to 70% over 40 minutes then for 5 minutes at 70% of ethyl acetate in heptane) and 210 mg (yield=33%) of expected product is obtained in the form of beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017637B2
Source datasetuspto-grants-2011_09
ORD IDord-96f27475666143159fa6838fd23f3ec9
Source noteuspto-grants-2011_09