Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 178502028 | HCID 178502028 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178502639 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05278181 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-d237d2daaa8b446381ab104ecc91b54f |
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| Source note | uspto-grants-1994_01 |
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