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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131603Generated: October 31, 2026

Pyridine → HCID 11315225, compound

https://huagongshe.com/reaction/131603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 21105720HCID 21105720—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11315225HCID 11315225—

Reaction Steps

N1-benzyl-4-methoxy-8-amino-dibenzo[b,d]furan-1-carboxamide (80 mg, 0.23 mmol) (step 2) was treated with acetyl chloride (1.1 eq.) in THF (10 ml) containing pyridine (1.0 eq) at 0° C. and allowed to warm to room temperature. The reaction was stirred at room temperature for 2 h. The reaction mixture was filtered and the filterarte was concentrated. The residue was triturated with ethanol to obtain 63 mg of N1-benzyl-4-methoxy-8-acetamido-dibenzo[b,d]furan-1-carboxamide as white solid; mp: 264-265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384962B2
Source datasetuspto-grants-2008_06
ORD IDord-9f332454a531471baf0af36e3ce7b224
Source noteuspto-grants-2008_06