HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 23447742, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Phenylthiourea | HCID 676454 | — |
| Reactant | HCID 23447840 | HCID 23447840 | — |
| Product | HCID 23447742 | HCID 23447742 | 69% |
Reaction Steps
Following the general procedure for protected phenyl thiourea formation outlined in example 12, N-[4-chloro-2-hydroxy-3-(N″,N″-dimethylaminosulfonyl)phenyl]-N′-(2-fluorophenyl)thiourea (440 mg, 1.09 mmol), tert-butyldimethylsilyl chloride (817 mg, 5.45 mmol) and imidazole (148 mg, 2.18 mmol) were reacted to form the desired product (387 mg, 69%). EI-MS m/z 518.2 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680317B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-cce430d25bda4fbdba778171c5be00f4 |
| Source note | uspto-grants-2004_01 |