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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350905Generated: November 2, 2026

Acetic Anhydride → HCID 178471579, compound

https://huagongshe.com/reaction/2350905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178471576HCID 178471576—
SolventFormic AcidHCID 284—
ProductHCID 178471579HCID 178471579—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1.0 g. (1.7 mmol) of diethyl N-[N-(2-pivaloylamino-4-hydroxypyrido[2,3-d]pyrimidin-6-ylmethyl)-4-aminomethylbenzoyl]-glutamate in 10 mL of 98% formic acid was added 0.35 g. (0.33 mL, 3.5 mmol) of acetic anhydride. The mixture was stirred at 25° C. for 1 h. The solvent was removed under reduced pressure and the solid dissolved in methylene chloride and extracted twice with a saturated solution of sodium bicarbonate. The aqueous layers were back extracted with methylene chloride, and the organic layers combined and dried over anhydrous magnesium sulfate. The solvent was evaporated to dryness to give a quantitative yield of diethyl N-[N-(2-pivaloylamino-4-hydroxypyrido[2,3-d]pyrimidin-6-ylmethyl)-N-formyl-4-aminomethylbenzoyl]-glutamate which can be employed for further processing without further purification; 1H NMR (Me2SO d6) delta 1.11-1.18 (m, 6H), 1.24 (s, 9H), 1.9-2.15 (m, 2H), 2.39-2.44 (m, 2H), 4.39-4.42 (m, 3H), 4.53-4.55 (m, 2H), 7.21-7.44 and 7.34-7.37 (m, 2H, AA'BB'), 7.76-7.78 and 7.81-7.84 (m, 2H, AA'BB'), 8.12 and 8.13 (s, 1H), 8.61-8.78 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871746
Source datasetuspto-grants-1989_10
ORD IDord-402be7e4c99545b3a2f434f177fa5575
Source noteuspto-grants-1989_10