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Methanol → HCID 178484913, 화합물

HRID 745259
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HRID 745259 반응식
Cl.C1(=O)[N:6]([CH2:7][C:8]2[CH:13]=[CH:12][C:11]([CH:14]=[CH:15][C:16]3[CH:25]=[CH:24][C:19]([C:20](=[NH:23])OC)=[CH:18][CH:17]=3)=[CH:10][CH:9]=2)[C:5](=[O:26])[C:4]2=[CH:27][CH:28]=[CH:29][CH:30]=[C:3]12.C(Cl)(Cl)[Cl:33].[CH3:36][OH:37].[CH3:38][NH2:39]>CCOCC>[ClH:33].[CH3:38][NH:39][C:20](=[NH:23])[C:19]1[CH:18]=[CH:17][C:16]([CH:15]=[CH:14][C:11]2[CH:12]=[CH:13][C:8]([CH2:7][N:6]3[C:36](=[O:37])[C:27]4=[CH:28][CH:29]=[CH:30][CH:3]=[C:4]4[C:5]3=[O:26])=[CH:9][CH:10]=2)=[CH:25][CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 6212ChloroformHCID 6329MethylamineHCID 70474423HCID 70474423, 화합물

생성물 1

HCID 178484913HCID 178484913, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To 1 g of methyl 4-[2-(4-phthalimidomethylphenyl)ethenyl]benzimidate hydrochloride, were added 60 ml of chloroform and 0.2 ml of a methanol solution containing 40% of methylamine. The mixture was stirred at room temperature for 15 hours and stripped of the solvent under reduced pressure. Ether was added to the residue and the precipitated crystals were collected by filtration to yield 0.33 g of N-methyl-4-[2-(4-phthalimidomethylphenyl)ethenyl]benzamidine hydrochloride; m.p. ≥280° C.

후처리

  1. filtrationthe precipitated crystals were collected by filtration

출처 및 근거

ORD 기록
ord-c47374660332453bad13723e44d6339c
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04598077

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