HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178419747, compound → HCID 178419718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178419747 | HCID 178419747 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178419718 | HCID 178419718 | 60% |
Reaction Steps
A mixture of 0.38 g (1.4 mmol) of 2-bromo-1-(4-imidazoyl)ethanone hydrobromide in 10 ml of acetone was warmed until homogeneous, then 0.17 g (1.4 mmol) of amidinothiourea was added and the mixture was heated at reflux for 0.5 hour. The mixture was cooled and the white precipitate was collected, washed with ether, and dried, thereby affording 0.24 g (60%) of 2-guanidino-4-(4-imidazoyl)thiazole hydrobromide, mp 225° (dec). nmr (DMSO-d6) (δ): 8.20 (s, 1H); 8.0 (b, 4H); 7.77 (s, 1H); 7.36 (s, 1H); high resolution mass spectrum: calcd. C7H8N6S: for 208.0531; found: 208.0517; calcd. for C7H8N6S.HBr.H2O: C, 27.37; H, 3.60; N, 27.36; found: C, 27.23; H, 3.57; N, 27.64.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374843 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-d39bbb69300547bc9618a0baad93a316 |
| Source note | uspto-grants-1983_02 |