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p-Toluenesulfonic acid monohydrate → HCID 178516181, 화합물

HRID 1846492
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HRID 1846492 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[NH:10][C:11]([CH:13]1[CH2:17][CH2:16][O:15][CH2:14]1)=O.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[Cl:9][C:4]1[C:3]2[NH:10][C:11]([CH:13]3[CH2:17][CH2:16][O:15][CH2:14]3)=[N:1][C:2]=2[CH:7]=[C:6]([OH:8])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 66978176N-(2-amino-6-chloro-4-hydroxyphenyl)tetrahydrofuran-3-carboxamide

생성물 1

HCID 178516181HCID 178516181, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

0.10 g (0.39 mmol) N-(2-amino-6-chloro-4-hydroxyphenyl)tetrahydrofuran-3-carboxamide were placed in 20 mL methanol, a spatula tip of p-toluenesulphonic acid monohydrate was added and the mixture was boiled for 2 h. The reaction mixture was evaporated down i.vac. and purified by chromatography. The fractions containing product were combined and evaporated down i.vac.

후처리

  1. customThe reaction mixture was evaporated down i.vac
  2. customand purified by chromatography
  3. additionThe fractions containing product
  4. customevaporated down i.vac

출처 및 근거

ORD 기록
ord-d47bc832bb53472b83595fbb6a198255
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952014B2

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