Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956516Generated: November 2, 2026

Morpholine → HCID 53851224, compound

https://huagongshe.com/reaction/1956516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPyBOPHCID 2724699—
ReactantHCID 69950775HCID 69950775—
SolventDichloromethaneHCID 6344—
ProductHCID 53851224HCID 53851224—

Reaction Steps

A mixture of 100 mg (0.163 mnmol) of 3-[2-[benzyloxycarbonyl-[4-(pyridin-4-yl)butyl]amino]ethyl]-2-(3,5 -dimethylphenyl)-1H-indole-5-carboxylic acid hydrochloride 101.7 mg (0.196 mmol) of PyBOP reagent, 0.085 mL (85.2 mg, 0.978 mmol) of morpholine, and 1 mL of dry methylene chloride was stirred under nitrogen at room temperature in a stoppered flask. After 5 days, the solution was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo. Purification of the crude product by flash chromatography on silica gel (gradient elution with 1-4% MeOH in CH2 Cl2) afforded a quantitative yield of the title compound as a yellow gum; homogeneous by TLC in 95:5 CH2Cl2 --MeOH. 500 MHz 1H NMR (CDCl3) was complex, owing to rotamners, but was consistent with the assigned structure. Mass spectrum (ESI): m/e=645.6 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780437
Source datasetuspto-grants-1998_07
ORD IDord-8435feb5c3f642119394430f026d83c4
Source noteuspto-grants-1998_07