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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloro-N,N-diethylacetamide | HCID 16844 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-2,4(1H,3H)-quinazolidinedione | HCID 133603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-1-(N,N-diethyl)aminocarbonylmethyl-2,4(1H, 3H)-quinazolinedione | HCID 12849425 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405623 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-97dbe4138d5f499da30a4d5802381c17 |
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| Source note | uspto-grants-1983_09 |
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