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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108744Generated: October 31, 2026

Bromoacetyl bromide → HCID 57421978, compound

https://huagongshe.com/reaction/2108744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantThioureaHCID 2723790—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 10307871—
ProductHCID 57421978HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514448B2
Source datasetuspto-grants-2009_04
ORD IDord-08436a6fefb2456ead33769ae6ad045a
Source noteuspto-grants-2009_04