HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → HCID 57421978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-methoxy-1H-pyrrolo[2,3-b]pyridine | HCID 10307871 | — |
| Product | HCID 57421978 | HCID 57421978 | — |
Reaction Steps
The title compound was synthesized in 2 steps in a manner similar to that described above using 5-methoxy-7-azaindole (0.37 g, 2.48 mmol), AlCl3 (1 g, 7.54 mmol), bromoacetylbromide (0.2 mL, 3 mmol) and thiourea (0.14 g, 1.88 mmol) (0.21 g, 39%, 2 steps) as a brown solid. Mass Spec.; MS 233 (M+1); 1H NMR(DMSO-d6, 500 MHz) δ 11.37 (s,1H), 9.10(s,1H), 7.86(d,1H), 7.70(d,1H), 7.61(d,1H), 6.88(s,2H), 6.67(s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514448B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-08436a6fefb2456ead33769ae6ad045a |
| Source note | uspto-grants-2009_04 |