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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197845Generated: October 31, 2026

Methanol → HCID 178502639, compound

https://huagongshe.com/reaction/1197845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium HydroxideHCID 14923—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 178502028HCID 178502028—
SolventWaterHCID 962—
ProductHCID 178502639HCID 178502639—

Reaction Steps

Methyl [5-(4-fluorobenzoyl)-1H-benzimidazol-2-yl]carbamate (Janssen Pharmaceutica, U.S. Pat. No. 3,657,267, Apr. 18, 1972) (31.61 g, 0.11 mole) and methoxylamine hydrochloride (0.35 mole) were added to abs. methanol. After heating under reflux for 48 hrs a clear solution was obtained. After 72 hrs this mixture was filtered hot through Celite then allowed to cool to room temperature. Removal of solvent under reduced pressure gave a solid residue. This material was suspended in H2O and adjusted to pH 12 with conc NH4OH. After stirring for 10 min the precipitate was isolated by filtration, washed repeatedly with H2O, then dried at 50° C. under reduced pressure to give the title product as a white solid. Yield: 33.08 g (96%). Mp: 290°-295° C., TLC: Rf=0.66,0.77 (CHCl3 --MeOH,10:1,SiO2) syn and anti isomers. IR (KBr): 3350, 2939, 1735 cm-1. 1H NMR (DMSO-d6): δ 3.73-3.75 (D, 3H, CH3); 3.85-3.87 (d, 3H, CH3); 6.95-7.46 (m, 7H, Ar); 11.74 (brd, s, 2 H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278181
Source datasetuspto-grants-1994_01
ORD IDord-d237d2daaa8b446381ab104ecc91b54f
Source noteuspto-grants-1994_01