HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → Des(N'-Methyl-2-nitro-1,1-ethenediaMino) N'-Methylureido Nizatidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazole | HCID 10977318 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Des(N'-Methyl-2-nitro-1,1-ethenediaMino) N'-Methylureido Nizatidine | HCID 13121954 | — |
Reaction Steps
Following the above reaction sequence, a solution of 0.93 g of 2-(2-dimethylaminomethyl-4-thiazolylmethylthio)ethylamine in 10 ml. of anhydrous acetonitrile was prepared. A solution of 0.22 ml. of methyl isocyanate in 5 ml. of anhydrous acetonitrile was added thereto. The reaction was stirred at ambient temperature for about 2.5 hours at which time the solvent was removed by evaporation. The resulting residue slowly crystallized and was recrystallized from cylcohexane to yield about 0.97 g of N-methyl-N'-2-(2-dimethylaminomethyl-4-thiazolylmethylthio)ethylurea melting at about 56°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382090 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-4483e5165f5a4b07b1fc147443e8454a |
| Source note | uspto-grants-1983_05 |