HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2H-1,4-Benzodiazepin-2-one, 5-(2-fluorophenyl)-1,3-dihydro-7-(hydroxyamino)-1-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Flunitrazepam | HCID 3380 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2H-1,4-Benzodiazepin-2-one, 5-(2-fluorophenyl)-1,3-dihydro-7-(hydroxyamino)-1-methyl- | HCID 148760 | — |
Reaction Steps
A mixture of 16 g. (0.05 mol) of 1,3-dihydro-5-(2-fluorophenyl)-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one, 500 ml. of tetrahydrofuran, 250 ml. of methanol, 68 g. of sodium acetate trihydrate and 56 g. of stannous chloride dihydrate was stirred under nitrogen for 6 hours. 25 ml. of concentrated ammonia was added and the inorganic salts were removed by filtration through celite. The filtrate was washed well with 2 l. of tetrahydrofuran. The filtrate was evaporated and the solid residue was dissolved in ethanol/tetrahydrofuran. The solution was again filtered with celite and concentrated. The separated crystals were collected to leave light yellow product. For analysis it was recrystallized from ethanol/tetrahydrofuran, m.p. 228°-230° dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989681 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-c19b7c4e77874a139a5e237a7526e80b |
| Source note | uspto-grants-1976_11 |