Hydrochloric Acid → N-[2-[4-Hydroxy-2-oxo-3H-1,3-benzothiazol-7-yl]ethyl]-2-[3-[2-[4-fluorophenyl]ethoxy]propylsulphonyl]acetamide

HRID 265306노트

반응식

HRID 265306 반응식
C(C1NC=CN=1)(C1NC=CN=1)=O.[F:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][O:22][CH2:23][CH2:24][CH2:25][S:26]([CH2:29][C:30]([OH:32])=O)(=[O:28])=[O:27])=[CH:16][CH:15]=1.Br.[NH2:34][CH2:35][CH2:36][C:37]1[C:45]2[S:44][C:43](=[O:46])[NH:42][C:41]=2[C:40]([OH:47])=[CH:39][CH:38]=1.Cl>CN(C=O)C.CCOCC.C(N(CC)CC)C>[OH:47][C:40]1[C:41]2[NH:42][C:43](=[O:46])[S:44][C:45]=2[C:37]([CH2:36][CH2:35][NH:34][C:30](=[O:32])[CH2:29][S:26]([CH2:25][CH2:24][CH2:23][O:22][CH2:21][CH2:20][C:17]2[CH:16]=[CH:15][C:14]([F:13])=[CH:19][CH:18]=2)(=[O:27])=[O:28])=[CH:38][CH:39]=1

참가 물질

8

실험 절차

Carbonyl diimidazole (1.94 g) was added to a stirred solution of the acid from step c) (3.64 g) in DMF (15 ml). Stirring was continued for 40 min at room temperature. To this solution was added 7-[2-aminoethyl]-4-hydroxy-1,3-benzothiazol-2(3H)-one hydrobromide (3.48 g) followed by triethylamine (1.7 ml). The whole was left overnight. The reaction mixture was then added slowly to a rapidly stirred mixture of 10% aqueous hydrochloric acid and ether (100 ml each). A pale yellow solid gradually settled out and was filtered off, washed with pentane and dried in vacuo. This provided the subtitled compound as a buff coloured material which was used in the next step without further purification.

후처리

  1. waitThe whole was left overnight
  2. filtrationwas filtered off
  3. washwashed with pentane
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-ef65cc57763e4535b5b46c82ac0e0166
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05648370

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