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Methyl iodide → HCID 178486086, 화합물

HRID 1758526
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인쇄 미리보기

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HRID 1758526 반응식
[CH3:1][NH:2][C:3]([N:5]1[CH2:14][C:13]2([CH2:18][C:17]3[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=3[O:15]2)[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[S:4].[I:23][CH3:24]>C(O)C.CO>[IH:23].[CH3:1][NH:2][C:3]([N:5]1[CH2:14][C:13]2([CH2:18][C:17]3[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=3[O:15]2)[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[SH:4][CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 132645342'(N-methylthiocarbamyl)spiro[benzofuran-2(3H), 4'(2'H)-isoquinoline]

생성물 1

HCID 178486086HCID 178486086, 화합물수율 93.8%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 887Methanol용매

실험 절차

A solution of 2'(N-methylthiocarbamyl)spiro[benzofuran-2(3H), 4'(2'H)-isoquinoline] (5.9 g) and iodomethane (4.1 g) in ethanol (45 ml) and methanol (100 ml) is heated under reflux overnight. Removal of the solvents yields a solid (8.1 g). The solid (1.0 g) is twice recrystallized from ethyl acetate/methanol to yield 0.6 g (60%) of product as crystals, mp 181°-182°.

후처리

  1. temperatureunder reflux overnight
  2. customRemoval of the solvents

출처 및 근거

ORD 기록
ord-a1d9ed61de7f44c58cc67ef11a852065
출처 데이터셋
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04374137

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