HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bismuth Citrate → N-[2-[[[5-[(Dimethylamino)methyl]-4-methyl-2-furanyl]methyl]-thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine 2-hydroxy-1,2,3-propanetricarboxylate bismuth
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bismuth Citrate | HCID 13135 | — |
| Reactant | N-[2-[[5-(Dimethylaminomethyl)-4-methyl-2-furanylmethyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine | HCID 67883984 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[2-[[[5-[(Dimethylamino)methyl]-4-methyl-2-furanyl]methyl]-thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine 2-hydroxy-1,2,3-propanetricarboxylate bismuth | HCID 73652917 | 64.2% |
Reaction Steps
To a solution of N-[2-[[[5-[(dimethylamino)methyl]-4-methyl-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine (6.465 g) in water (25 ml) was added bismuth citrate (7.84 g) and the mixture heated at 100° for 4 hours. The suspension was filtered and the residue washed well with water then ethanol and dried to give a solid consisting of unchanged bismuth citrate (2.448 g) which was discarded. The combined filtrate and washings were evaporated to dryness with the aid of methanol (3×50 ml) then ethanol (2×50 ml). The residue was mixed with cold ethanol (70 ml) and triturated to a fine cream which was filtered off, washed with ethanol (4×5 ml) and then ether and dried to give the title compound (9.187 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05229418 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-c4a5c36c0ae247f2a4ecf7b1fa5dd665 |
| Source note | uspto-grants-1993_07 |