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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995646Generated: October 29, 2026

Chloro-N,N-diethylacetamide → 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-1-(N,N-diethyl)aminocarbonylmethyl-2,4(1H, 3H)-quinazolinedione

https://huagongshe.com/reaction/1995646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloro-N,N-diethylacetamideHCID 16844—
ReactantSodium hydrideHCID 24758—
Reactant3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-2,4(1H,3H)-quinazolidinedioneHCID 133603—
SolventDimethylformamideHCID 6228—
Product3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-1-(N,N-diethyl)aminocarbonylmethyl-2,4(1H, 3H)-quinazolinedioneHCID 1284942557%

Reaction Conditions

Temperature80 °C

Reaction Steps

A portion (30 mg) of sodium hydride suspension (50%) in mineral oil was added to a stirred solution of 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-2,4-(1H, 3H)-quinazolinedione (187 mg) in dimethylformamide (10 ml). After addition of N,N-diethyl-chloroacetamide (80 mg), the mixture was stirred at 80° C. for 3 hours. The solvent was evaporated off at reduced pressure, and the residue was extracted with CHCl3. The CHCl3 extract was washed with water, dried over NaSO4 and concentrated. The residue was recrystallized from methanol to give 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-1-(N,N-diethyl)aminocarbonylmethyl-2,4(1H, 3H)-quinazolinedione (138 mg, 57%) melting at 228°-229° C. MS: M/e, 485(M+), 450. NMR: δ (ppm, CDCl3), 1.38 (9H, m), 2.39 (3H, s), 2.72 (3H, s), 3.45 (4H, q), 4.40 (2H, q), 4.95 (2H, d), 6.75 (1H, s), 7.40 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405623
Source datasetuspto-grants-1983_09
ORD IDord-97dbe4138d5f499da30a4d5802381c17
Source noteuspto-grants-1983_09