Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642693Generated: October 30, 2026

Methylamine → 5-fluoro-3-methylaminomethyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant5-fluoro-3-formyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl esterHCID 86613189—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-fluoro-3-methylaminomethyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl esterHCID 68578519—

Reaction Steps

To a solution of 5-fluoro-3-formyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester (from Example 76.1., 0.60 g) in MeOH (5.0 ml), AcOH (0.92 ml), tetrahydrofuran (2.0 ml) and methyl amine (2 M in THF, 3.2 ml) was added portion wise Na(CN)BH3 (202 mg) and stirring was continued at 22° C. for 3 h. The mixture was evaporated and the residue partitioned between 1 N aqueous HCl and dichlormethane. The pH of the aqueous layer was adjusted to 11 using NaOH, extracted with dichloromethane, dried and evaporated to give 5-fluoro-3-methylaminomethyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester as a colorless oil. MS: 391.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696240B2
Source datasetuspto-grants-2010_04
ORD IDord-44ef5d1acc1e49ef91186bcc119b69ee
Source noteuspto-grants-2010_04