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Dichloromethane → HCID 66748038, 화합물

HRID 2402143
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반응식

HRID 2402143 반응식
[C:1]([C:3]1[C:4]([CH3:18])=[C:5]([C:14]([O:16][CH3:17])=[O:15])[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2].C(Cl)Cl.[Br:22]Br>>[Br:22][CH2:18][C:4]1[C:3]([C:1]#[N:2])=[C:7]([N:8]2[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)[S:6][C:5]=1[C:14]([O:16][CH3:17])=[O:15]
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참가 물질

4

반응물 3

HCID 6344Dichloromethane2회HCID 24408BromineHCID 66747691HCID 66747691, 화합물

생성물 1

HCID 66748038HCID 66748038, 화합물수율 96.6%

실험 절차

To the solution of methyl 4-cyano-3-methyl-5-(morpholin-4-yl)thiophene-2-carboxylate (0.500 g, 1.88 mmol) in anhydrous methylene chloride (15 mL, 230 mmol) was added a solution of bromine (0.409 g, 2.56 mmol) in anhydrous methylene chloride (5.0 mL, 78 mmol). The mixture was stirred at room temperature for 4 days. The mixture was evaporated under reduced pressure and dried in vacuum to give a crude product that was used without further purification (0.658 g, contained 3.4% starting material, yield 96.6%). LC/MS: (FA) ES+ 345, 347. 1H NMR (400 MHz, d-chloroform) δ 4.83 (s, 2H), 3.87 (s, 3H), 3.85 (m, 4H), 3.62 (m, 4H).

후처리

  1. customThe mixture was evaporated under reduced pressure
  2. customdried in vacuum

출처 및 근거

ORD 기록
ord-621f20e333d04c8db0cd34da50421111
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796271B2

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