HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 178486148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 23447819 | HCID 23447819 | — |
| Reactant | HCID 178418324 | HCID 178418324 | — |
| Product | HCID 178486148 | HCID 178486148 | 40% |
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-fluorophenyl)carbodiimide (350 mg, 0.72 mmol), cyanamide (121 mg, 2.88 mmol) and N,N-diisopropylethylamine (111 mg, 0.86 mmol) were reacted, followed by desilylation with Cesium fluoride (132 mg, 0.86 mmol) to form the desired product (120 mg, 40%). EI-MS m/z 412.2 (M+). 1H NMR (DMSO-d6) δ 2.86 (s, 6H), 7.20 (m, 2H), 7.27 (m, 2H), 7.40 (t, 1H), 7.52 (d, 1H), 9.06 (s, 1H), 9.20 (s, 1H), 10.51 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680317B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-2f43855568e94d89840e1355de363fb7 |
| Source note | uspto-grants-2004_01 |