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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182226Generated: October 31, 2026

Acetic Anhydride → HCID 22477457, compound

https://huagongshe.com/reaction/2182226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178427315HCID 178427315—
SolventTolueneHCID 1140—
ProductHCID 22477457HCID 2247745743.4%

Reaction Steps

To a suspension of N-hydroxy-1-methyl-3-[1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-1H-indole-5carboxamidine [0.7 g, Reference Example 26] in toluene (30 mL) at ambient temperature under nitrogen was added acetic anhydride (0.467 g). The reaction mixture was heated at reflux for 4.5 hours then filtered. The filtrate was evaporated to give the title compound (0.32 g) as a dark red oil which was used immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897207B2
Source datasetuspto-grants-2005_05
ORD IDord-09788e9fa1ca453eb232a7e9dec7a12e
Source noteuspto-grants-2005_05