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3-Amino-1-phenylpropan-1-ol → HCID 21510116, 화합물

HRID 1658268
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HRID 1658268 반응식
[NH2:1][CH2:2][CH2:3][CH:4]([OH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.N([C:16]1[NH:17][CH2:18][CH2:19][CH2:20][N:21]=1)[N+]([O-])=O>C1(C)C(C)=CC=CC=1>[NH:21]1[CH2:20][CH2:19][CH2:18][N:17]=[C:16]1[NH:1][CH2:2][CH2:3][CH:4]([OH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1215483-Amino-1-phenylpropan-1-olHCID 412214N-(1,4,5,6-Tetrahydropyrimidin-2-yl)nitramide

생성물 1

HCID 21510116HCID 21510116, 화합물

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of 8 parts of α(2-aminoethyl)benzylalcohol, 7.2 parts of 2-(nitramino)- 1,4,5,6-tetrahydropyrimidine and 40 parts of xylene is stirred and refluxed for 48 hours with waterseparator. Upon cooling the reaction mixture, the product is separated as an oil. The xylene is decanted and the oily product is triturated in diisopropylether. The solid product is filtered off and crystallized from acetone, yielding α-[2-(1,4,5,6-tetrahydro-2-pyrimidinylamino)ethyl]benzylalcohol; m.p. 130°-135°C.

후처리

  1. temperaturerefluxed for 48 hours with waterseparator
  2. temperatureUpon cooling the reaction mixture
  3. customthe product is separated as an oil
  4. customThe xylene is decanted
  5. customthe oily product is triturated in diisopropylether
  6. filtrationThe solid product is filtered off
  7. customcrystallized from acetone

출처 및 근거

ORD 기록
ord-6bbebc4e748141e9a26f7b6ce9579a5c
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03963718

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