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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639532Generated: October 30, 2026

4-Methylmorpholine → HCID 24760641, compound

https://huagongshe.com/reaction/639532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPotassium HydroxideHCID 14797—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 68576716HCID 68576716—
ReactantHCID 68579087HCID 68579087—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24760641HCID 2476064174.4%

Reaction Steps

A solution of 4-fluoro-1H-pyrrolo[2,3-c]pyridine-7-carboxylic acid ethyl ester (50 mg, 0.24 mmol) in THF (0.7 mL) was treated with 2 M aq. potassium hydroxide solution (0.24 mL, 0.48 mmol) and stirred for 90 min at RT. The reaction mixture was then evaporated, the residue dissolved in DMF (3.2 mL) and treated with (4-tert-butyl-benzyl)-[2-(4-chloro-3-trifluoromethyl-phenyl)-ethyl]-amine (98 mg, 0.26 mmol), N-methylmorpholine (73 mg, 0.72 mmol), and HBTU (137 mg, 0.36 mmol). After 16 h, the reaction mixture was partitioned between water and ethyl acetate, the organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography of the residue (SiO2, heptane/ethyl acetate 97:3) afforded the title compound (95 mg, 74%). White foam, MS (ISP) 532.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691876B2
Source datasetuspto-grants-2010_04
ORD IDord-75cc8eab17de46f8bc11716e7c1c12fe
Source noteuspto-grants-2010_04