HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(3-Aminopropoxy)-N,N-dimethylbenzenemethanamine → N-[3-[3-[(Dimethylamino)methyl]phenoxy]propyl]-N'-[2-[[5-[(methylamino)methyl]-2-furanylmethyl]thio]ethyl]-2-nitro-1,1-ethenediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(3-Aminopropoxy)-N,N-dimethylbenzenemethanamine | HCID 12913950 | — |
| Reactant | 1-Nitro-2-methylthio-2-{2-[(5-methylaminomethyl-2-furyl)methylthio]ethylamino}ethylene | HCID 70538398 | — |
| Product | N-[3-[3-[(Dimethylamino)methyl]phenoxy]propyl]-N'-[2-[[5-[(methylamino)methyl]-2-furanylmethyl]thio]ethyl]-2-nitro-1,1-ethenediamine | HCID 70538242 | — |
Reaction Steps
A mixture of N-methyl-5-[[[2-[(1-methylthio-2-nitroethenyl)amino]ethyl]thio]methyl]-2-furanmethanamine (1.6 g) (prepared from the oxalate salt) and 3-(3-aminopropoxy)-N,N-dimethylbenzenemethanamine (1.15 g) was heated at 98°-100° for 3 hours. The oily product was chromatographed (silica/methanol-0.88 ammonia 79:1) and the appropriate eluate evaporated to dryness to give the title compound as a hydrate as an amber oil (2.12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233302 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-4303ae74ac7842a8b3c04667c62708dd |
| Source note | uspto-grants-1980_11 |