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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073550Generated: October 30, 2026

Acetic Anhydride → HCID 53642917, compound

https://huagongshe.com/reaction/2073550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 73654802HCID 73654802—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 53642917HCID 5364291785%

Reaction Steps

A solution of methyl 4-[2-[5-(N-cyclopentylmethylcarbamoyl)-2-methylaminophenyl]-2-(hydroxyimino)ethyl]-3-methoxybenzoate (79.9 mg), 4-(dimethylamino)pyridine (22 mg), and acetic anhydride (0.17 ml) in dichloromethane (11 ml) was stirred under a nitrogen atmosphere for 15 hours. The solution was diluted with dichloromethane, washed with 5% w/v sodium hydrogen sulfate, water, and brine, then dried (MgSO4), and evaporated to give methyl 4-[2-(acetoxyimino)-2-[5-(N-cyclopentylmethylcarbamoyl)-2-methylaminophenyl]ethyl]-3-methoxybenzoate (74.1 mg, 85%) as a pink solid; NMR (80 MHz, CDCl3): 1.2-1.8[8H, (CH2)4 ], 2.1(s, 3H, CH3CO), 3.0(d, 3H, NCH3), 3.3(dd, 2H, CH2NH), 3.9(2s, 6H, 2×OCH3), 4.3(s, 2H, ArCH2), 5.8(broad, 1H, NHCO), 6.7(d, 1H), 7.0(d, 1H), 7.4-7.6(m, 3H), 7.8(d, 1H), 8.5(broad, 1H, CH3NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918094
Source datasetuspto-grants-1990_04
ORD IDord-df6e224fa7be473db467176dc12a5589
Source noteuspto-grants-1990_04