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HCID 58012209, 화합물 → 5-(5-chloro-2-thienyl)-1-(2-fluorobenzyl)-1,3-dihydro-2H-imidazol-2-one

HRID 660908
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반응식

HRID 660908 반응식
[Cl:1][C:2]1[S:6][C:5]([C:7](=O)[CH2:8][NH:9][C:10]([NH:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[F:20])=[O:11])=[CH:4][CH:3]=1>Cl.CO>[Cl:1][C:2]1[S:6][C:5]([C:7]2[N:12]([CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[F:20])[C:10](=[O:11])[NH:9][CH:8]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 58012209HCID 58012209, 화합물

생성물 1

HCID 580122955-(5-chloro-2-thienyl)-1-(2-fluorobenzyl)-1,3-dihydro-2H-imidazol-2-one

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 887Methanol용매

실험 절차

1300 mg (ca. 4.0 mmol) of 1-[2-(5-chloro-2-thienyl)-2-oxoethyl]-3-(2-fluorobenzyl)-urea (Example 235A) are suspended in 15 ml of concentrated hydrochloric acid, diluted with 15 ml of methanol diluted and stirred at RT for 2 hrs. The suspension is filtered, the filtrate concentrated in vacuo and the residue purified by preparative HPLC [Method 10]. 220 mg (18% of theory) of the target compound are thus obtained.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. additiondiluted
  2. filtrationThe suspension is filtered
  3. concentrationthe filtrate concentrated in vacuo
  4. customthe residue purified by preparative HPLC [Method 10]
  5. custom220 mg (18% of theory) of the target compound are thus obtained

출처 및 근거

ORD 기록
ord-cca2c5591ae94ff5b2dffacddf848a4c
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084481B2

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