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Methylamine → HCID 9864602, 화합물

HRID 1250949
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HRID 1250949 반응식
[CH:1]1[C:6]2[CH:7]=[C:8]3[C:22](=[O:23])[O:21][CH2:20][C:9]3=[C:10]([C:11]3[CH:12]=[CH:13][C:14]4[O:19][CH2:18][O:17][C:15]=4[CH:16]=3)[C:5]=2[C:4]2[O:24][CH2:25][O:26][C:3]=2[CH:2]=1.[CH3:27][NH2:28]>C1C=CC=CC=1>[CH3:27][NH:28][C:22]([C:8]1[CH:7]=[C:6]2[C:5](=[C:10]([C:11]3[CH:12]=[CH:13][C:14]4[O:19][CH2:18][O:17][C:15]=4[CH:16]=3)[C:9]=1[CH2:20][OH:21])[C:4]1[O:24][CH2:25][O:26][C:3]=1[CH:2]=[CH:1]2)=[O:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 177023Helioxanthin

생성물 1

HCID 9864602HCID 9864602, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

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온도
120 °C

실험 절차

Helioxanthin (1.0 g) was suspended in benzene (10 ml), followed by addition of methylamine (40% methanol solution: 2 ml). The mixture was heated at 120° C. under stirring for 4 days. The reaction mixture was concentrated under reduced pressure. The resulting residue was recrystalized from DMF to yield the title compound (144 mg).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customThe resulting residue was recrystalized from DMF

출처 및 근거

ORD 기록
ord-ca3e1b4690e341a4af366c7823cacc25
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06340704B1

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