HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 178486151, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | HCID 23447837 | HCID 23447837 | — |
| Reactant | HCID 178418324 | HCID 178418324 | — |
| Product | HCID 178486151 | HCID 178486151 | 3.4% |
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′-(2,3-difluorophenyl)carbodiimide (340 mg, 0.68 mmol), cyanamide (114 mg, 2.72 mmol) and N,N-disopropylethylamine (106 mg, 0.82 mmol) were reacted, followed by desilylation with Cesium fluoride (124 mg, 0.82 mmol) to form the desired product (10 mg, 3.4%). EI-MS m/z 430.0 (M+). 1H NMR (DMSO-d6) δ 2.87 (s, 6H), 7.21 (m, 3H), 7.30 (m, 1H), 7.54 (d, 1H), 9.2 (s, 1H), 10.54 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680317B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-d7f0644e007c4956b9cb8c2e0d06b799 |
| Source note | uspto-grants-2004_01 |