HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(7-Acetylenyl-2-benzothiazolyl)-3-ethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N,N-dimethylformamide methanol | HCID 21901440 | — |
| Reactant | 1-(7-Trimethylsilylacetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985538 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1-(7-Acetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985650 | 15.3% |
Reaction Steps
A mixture of 1-(7-trimethylsilylacetylenyl-2-benzothiazolyl)-3-ethylurea 2 (0.050 g, 0.16 mmol) and 1M aqueous KOH solution (0.16 mL, 0.16 mmol, 1.0 eq) in 1.5 mL of 2/1 mixture of DMF/MeOH was stirred at room temperature for about 2 hours. The mixture was taken up in 10 mL MeOH and the precipitation was filtered off. The mother liquid was concentrated and purified by prep HPLC to give the desired compound 0.006 g (15%). LC/MS 246 (M+1); LC retention time 2.77 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091227B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-8abe128357e5495cb8583bed1bcfdda2 |
| Source note | uspto-grants-2006_08 |