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Triethylamine → HCID 131728995, 화합물

HRID 1010540
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HRID 1010540 반응식
[NH2:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][NH:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].CS[C:17](SC)=[CH:18][N+:19]([O-:21])=[O:20].C(N(CC)CC)C>C(#N)C>[C:11]([O:10][C:8]([NH:7][CH2:6][CH2:5][N:4]1[CH2:3][CH2:2][NH:1][C:17]1=[CH:18][N+:19]([O-:21])=[O:20])=[O:9])([CH3:14])([CH3:13])[CH3:12]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 836231,1-Bis(methylthio)-2-nitroethyleneHCID 3621142N1-Boc-2,2'-iminodiethylamine

생성물 1

HCID 131728995HCID 131728995, 화합물수율 64.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A stirred mixture of 2.03 gram (0.010 mole) of N-{2-[(2-aminoethyl)amino]ethyl}(tert-butoxy)carboxamide (commercially available), 1.18 gram (0.010 mole) of 1,1-di(methylthio)-2-nitroethene and 2 mL (excess) of triethylamine in 40 mL of acetonitrile was warmed to reflux where it was maintained for four hours. After this time the reaction mixture was concentrated under reduced pressure to a solid residue. The residue was washed with diethyl ether and dried, yielding 1.76 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

후처리

  1. temperaturewas warmed
  2. temperatureto reflux where it
  3. temperaturewas maintained for four hours
  4. concentrationAfter this time the reaction mixture was concentrated under reduced pressure to a solid residue
  5. washThe residue was washed with diethyl ether
  6. customdried

출처 및 근거

ORD 기록
ord-83fbfe82ef324b09bb1c32567922b592
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977332B2

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