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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388309Generated: November 2, 2026

Acetic Anhydride → HCID 59541780, compound

https://huagongshe.com/reaction/2388309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 59464242HCID 59464242—
SolventDichloromethaneHCID 6344—
ProductHCID 59541780HCID 59541780—

Reaction Steps

6-(1,4-Dioxa-spiro[4.5]dec-8-yl)-pyridin-3-ylamine (0.158 g, 0.675 mmol, prepared as described in Example 3: Steps A-B from 5-amino-2-bromopyridine, Aldrich) was dissolved in anhydrous dichloromethane (10 mL), treated with acetic anhydride (Aldrich, 0.080 mL, 0.846 mmol), and stirred at ambient temperature under Ar for 18 h. The reaction was quenched with saturated aqueous NaHCO3, extracted thrice with dichloromethane, and the combined organic layers washed with brine, dried over Na2SO4, filtered, and the filtrate concentrated in vacuo giving the title compound as a pale solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269015B2
Source datasetuspto-grants-2012_09
ORD IDord-23acb763b88b4b1c9243eab341a13fcb
Source noteuspto-grants-2012_09