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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835221Generated: November 2, 2026

Acetic Anhydride → HCID 22477457, compound

https://huagongshe.com/reaction/1835221

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-5-carboxamidine [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 numberUS06770643B2
Source datasetuspto-grants-2004_08
ORD IDord-9baa3fbfffcd43eb97e348e6ceb446a3
Source noteuspto-grants-2004_08