Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067996Generated: November 1, 2026

3-Fluorobenzylamine → HCID 58055090, compound

https://huagongshe.com/reaction/2067996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzylamineHCID 66853—
Reactant2-Thiazolamine, 4-(chloromethyl)-, hydrochloride (1:1)HCID 73228—
ReactantDiisopropylethylamineHCID 81531—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58055090HCID 5805509058%

Reaction Steps

A stirred mixture of Intermediate 1: 4-(chloromethyl)thiazol-2-amine hydrochloride (27.8 g, 0.15 mol), carbonyl diimidazole (25.5 g, 0.157 mol), and anhydrous THF (0.2 L) was treated dropwise with a solution of DIPEA (26.2 mL, 0.15 mol) in THF (20 mL) at 20-30° C. After 2-3 hours stifling, a solution of 3-fluorobenzylamine (18.5 mL, 0.164 mol) in THF (40 mL) was added. The reaction was diluted with water (200 mL) and THF was evaporated under reduced pressure. The residue was extracted with DCM (2×200 mL). The combined extracts were dried over sodium sulfate and concentrated to leave an orange resin that was purified by silica gel chromatography (acetone/hexane) to afford Intermediate 4 as a pale yellow solid (26 g, 58% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293919B2
Source datasetuspto-grants-2012_10
ORD IDord-3f8266bca2554f539faf2dac6be40479
Source noteuspto-grants-2012_10