HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 178486152, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 23447853 | HCID 23447853 | — |
| Reactant | HCID 178418324 | HCID 178418324 | — |
| Product | HCID 178486152 | HCID 178486152 | 50% |
Reaction Steps
Following the general procedure for cyanoguanidine formation outlined in example 12, N-[4-chloro-2-tert-butyldimethylsilyloxy-3-(N″,N″-dimethylaminosulfonyl)phenyl]N′-(2-chloro4-fluorophenyl)carbodiimide (420 mg, 0.81 mmol), cyanamide (136 mg, 3.24 mmol) and N,N-diisopropylethylamine (126 mg, 1.62 mmol) were reacted, followed by desilylation with Cesium fluoride (148 mg, 1.62 mmol) to form the desired product (180 mg, 50%). EI-MS m/z 446.2 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680317B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-778b99eb1dae4375a414a5021de79ab9 |
| Source note | uspto-grants-2004_01 |