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Monoethyl malonate → HCID 178516622, 화합물

HRID 41753
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HRID 41753 반응식
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([NH2:10])=[CH:9][C:4]=2[N:3]=[CH:2]1.[F:11][C:12]1([F:26])[CH2:17][CH2:16][N:15]([C:18]2[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=2)[CH2:14][CH2:13]1.C([O:29][C:30]([CH2:32][C:33](O)=[O:34])=O)C.C(=O)(OC)OC(C)(C)C[N+]#[C-].CC(C)([O-])C.[Na+]>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([N:10]3[CH:22]([C:21]4[CH:24]=[CH:25][C:18]([N:15]5[CH2:16][CH2:17][C:12]([F:26])([F:11])[CH2:13][CH2:14]5)=[CH:19][CH:20]=4)[C:30](=[O:29])[CH2:32][C:33]3=[O:34])=[CH:9][C:4]=2[N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 70615Monoethyl malonateHCID 23676156Sodium t-butoxideHCID 252674641-Isocyano-2-methylpropan-2-yl methyl carbonateHCID 866708774-(4,4-Difluoropiperidin-1-yl)benzaldehydeHCID 178507353HCID 178507353, 화합물

생성물 1

HCID 178516622HCID 178516622, 화합물

실험 절차

The compound was synthesized starting from 1H-benzo[d]imidazol-5-amine (0.890 g, 6.69 mmol), 4-(4,4-difluoropiperidin-1-yl)benzaldehyde (1.5 g, 6.69 mmol), 2-(ethoxycarbonyl)acetic acid (0.883 g, 6.69 mmol), 1-isocyano-2-methylpropan-2-yl methyl carbonate (1.05 g, 6.69 mmol) and sodium tert.-butoxide (0.713 g, 6.35 mmol) according to method 3.

후처리

  1. customThe compound was synthesized

출처 및 근거

ORD 기록
ord-04d66ba45c82473a8f4ab8194da2842e
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530670B2

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