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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898362Generated: October 31, 2026

4-Methylmorpholine → HCID 178446461, compound

https://huagongshe.com/reaction/1898362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPentylamineHCID 8060—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 178422813HCID 178422813—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178446461HCID 17844646130.4%

Reaction Steps

The title compound was prepared following the procedure as described for Example-1 using 2-[(2,6-dichlorophenyl)amino]-7,7-dimethyl-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxylic acid (Intermediate-6, 0.070 g, 0.178 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (0.114 g, 0.306 mmol), N-methyl morpholine (1.0 mL), DMF (1.0 mL), THF (5.0 mL) and pentan-1-amine (0.031 g, 0.356 mmol) to afford 0.025 g of the desired product. 1HNMR (DMSO-d6): δ 0.880 (m, 3H), 1.23-1.33 (m, 8H), 1.49 (s, 6H), 3.03 (s, 2H), 7.19 (m, 1H), 7.32 (s, 1H), 7.50 (d, J=7.8 Hz, 2H), 7.71 (s, 1H), 10.50-11 (s, 2H); MS [M+H]+: 461.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-76c5499a67dc4abfa27851cb4e6693f1
Source noteuspto-grants-2013_08