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Butylamine → HCID 178449171, 화합물

HRID 1492296
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HRID 1492296 반응식
[CH3:1][N:2]=[C:3]=[N:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1.[CH2:17]([NH2:21])[CH2:18][CH2:19][CH3:20]>C(O)(C)(C)C>[CH2:17]([NH:21][C:3]([NH:2][CH3:1])=[N:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1)[CH2:18][CH2:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8007ButylamineHCID 15746469N-methyl-N'-(2-morpholinophenyl)carbodiimide

생성물 1

HCID 178449171HCID 178449171, 화합물

시약·촉매·용매 1

HCID 6386tert-Butanol용매

실험 절차

A mixture of N-methyl-N'-(2-morpholinophenyl)carbodiimide (1 g), n-butylamine (0.5 g) and t-butanol (5 ml) was heated at 90°-95° C. for four hours. The solvent was removed by evaporation and the residue dissolved in dichloromethane (100 ml) and the resulting solution was washed with water, dried and filtered. Removal of the solvent gave 1-(n-butyl)-2-(2-morpholinophenyl)-3-methylguanidine which was converted into its monofumarate salt (m.p. 178°-179° C.).

후처리

  1. temperaturewas heated at 90°-95° C. for four hours
  2. customThe solvent was removed by evaporation
  3. dissolutionthe residue dissolved in dichloromethane (100 ml)
  4. washthe resulting solution was washed with water
  5. customdried
  6. filtrationfiltered
  7. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-2a478b8d14234aa2881061184716c589
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05373008

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