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2-Methylpropylenediamine → HCID 22147743, 화합물

HRID 1824311
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HRID 1824311 반응식
[C:1]([C:3]1[CH:18]=[CH:17][C:6]([O:7][C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=O)=[CH:10][CH:9]=2)=[CH:5][CH:4]=1)#[N:2].[NH2:19][CH2:20][C:21]([NH2:24])([CH3:23])[CH3:22]>C1COCC1>[NH2:24][C:21]([CH3:23])([CH3:22])[CH2:20][NH:19][C:12](=[O:14])[C:11]1[CH:10]=[CH:9][C:8]([O:7][C:6]2[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:18][CH:17]=2)=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 131282-MethylpropylenediamineHCID 21798064-(4-cyanophenoxy)benzoic acid

생성물 1

HCID 22147743HCID 22147743, 화합물수율 38.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

4-(4′-Cyanophenoxy)benzoic acid (1.00 g, 4.2 mmol) was dissolved in THF (40 mL) followed by the addition of 1,1-carbonyldiimidazole (0.745 g, 4.6 mmol) in small portions. This mixture was stirred for 1 hour whereupon 1,2-diamino-2-methylpropane (0.48 mL, 4.6 mmol) was added and the resultant mixture stirred for 20 hours at RT. The mixture was then concentrated in vacuo and the residue chromatographed over silica (10% MeOH/CHCl3) to provide 0.50 g (38%) of the desired product. MS. (FD+) 310.2 m.p. 133–137° C.

후처리

  1. additionwas added
  2. concentrationThe mixture was then concentrated in vacuo
  3. customthe residue chromatographed over silica (10% MeOH/CHCl3)

출처 및 근거

ORD 기록
ord-c4c14ba085a24f2181e162cbeec8a31f
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07041684B2

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