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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896637Generated: November 1, 2026

N-bromobutanimide → HCID 86654218, compound

https://huagongshe.com/reaction/1896637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67135536HCID 67135536—
SolventAcetonitrileHCID 6342—
ProductHCID 86654218HCID 86654218100.2%

Reaction Steps

3-Chloro-5-amino-2-(2,2,2-trifluoroethoxy)-pyridine (3.05 g) obtained in Step B was brominated with N-bromosuccinimide (2.4 g) in acetonitrile (68 ml) as described in Example 14, Step C to give 2-bromo-5-chloro-6-trifluoroethoxy-pyridin-3-yl-amine (4.12 g) as a red oil. MS (ES+) 305/307/309 (MH+); 346/348/350 (MH++CH3CN); 1H NMR (400 MHz, CDCl3) 3.80 (br s, 2H), 4.65 (q, 2H), 7.10 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518971B2
Source datasetuspto-grants-2013_08
ORD IDord-96894b3986a1491399ffef0efe495791
Source noteuspto-grants-2013_08