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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362306Generated: November 1, 2026

Methylamine → (3-Chloro-7-fluoro-benzo[b]thiophen-2-ylmethyl)methylamine

https://huagongshe.com/reaction/1362306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Chloro-7-fluoro-benzo[b]thiophene-2-carbaldehydeHCID 59277554—
SolventMethanolHCID 887—
Product(3-Chloro-7-fluoro-benzo[b]thiophen-2-ylmethyl)methylamineHCID 5927754970%

Reaction Steps

A solution of 3-chloro-7-fluoro-benzo[b]thiophene-2-carbaldehyde (610 mg, 2.78 mmol) in CH3NH2 (20 mL of a 2.0 M solution in MeOH, 40 mmol) was stirred at room temperature overnight. The mixture was concentrated. The residue was dissolved in EtOH (20 mL), and after cooling in an ice bath, NaBH4 (159 mg, 4.20 mmol) was added. The mixture was slowly warmed to room temperature and then stirred overnight. The mixture was concentrated. The residue was taken up in NaOH (20 mL) and the mixture extracted with Et2O (3×). The combined organics were washed with satd NaCl, dried (Na2SO4) and concentrated. Purification by column chromatography (silica gel, 95:5 CH2Cl2/MeOH) gave the title compound (460 g, 70%) as a brown oil: 1H NMR (300 MHz, CDCl3) δ 7.56 (d, J=8.0 Hz, 1H), 7.38 (ddd, J=7.9, 7.9, 4.9 Hz, 1H), 7.06 (dd, J=8.8, 8.8 Hz, 1H), 4.09 (s, 2H), 2.53 (s, 3H), 1.55 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-74a30b0ccff74e0bb160c682c2b1af74
Source noteuspto-grants-2011_02