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Urea → HCID 53784406, 화합물

HRID 1905691
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HRID 1905691 반응식
[CH3:1][O:2][C:3]([N:5]1[CH2:9][C:8]([N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[C:7]([C:15](=[O:22])[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:6]1)=[O:4].CO[CH:25](OC)[N:26]([CH3:28])[CH3:27].NC(N)=O>O1CCOCC1>[CH3:1][O:2][C:3]([N:5]1[CH2:9][C:8]([N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[C:7]([C:15](=[O:22])[C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:25][N:26]([CH3:28])[CH3:27])[CH2:6]1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1176UreaHCID 78373Dimethylformamide dimethyl acetalHCID 21270415HCID 21270415, 화합물

생성물 1

HCID 53784406HCID 53784406, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 12.41 g of N-methoxycarbonyl-3-carboethoxyacetyl-4-pyrrolidino-2,5-dihydropyrrole, 9.64 ml of N,N-dimethylformamide dimethylacetal and 10 mg of urea in 50 ml of dioxane is stirred under nitrogen for 16 hours. Evaporation of the solvent yields N-methoxycarbonyl-3-(2-ethoxycarbonyl-3-dimethylaminoacryloyl)-4-pyrrolidino-2,5-dihydropyrrole as an oil.

후처리

  1. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-6f3315b802a44110ad56ae9c54ec2325
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04647566

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