Hydroxylamine → 4-Cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-yl-N-(tetrahydro-2H-pyran-2-yloxy)thiophene-2-carboxamide

HRID 572629노트

반응식

HRID 572629 반응식
[C:1]([C:3]1[C:4]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][C:18]=2[Cl:24])=[C:5]([C:14]([OH:16])=O)[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2].CN(C(ON1N=N[C:35]2[CH:36]=[CH:37][CH:38]=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C.[NH2:58][OH:59].CN([CH:63]=[O:64])C>>[C:1]([C:3]1[C:4]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][C:18]=2[Cl:24])=[C:5]([C:14]([NH:58][O:59][CH:38]2[CH2:37][CH2:36][CH2:35][CH2:63][O:64]2)=[O:16])[S:6][C:7]=1[N:8]1[CH2:9][CH2:10][O:11][CH2:12][CH2:13]1)#[N:2]

참가 물질

6

실험 절차

4-Cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylic acid (0.080 g, 0.21 mmol), HATU (0.095 g, 0.25 mmol), and diisopropylethylamine (0.073 mL, 0.42 mmol) were dissolved in DMF (2 mL) and stirred for 30 minutes. O-Tetrahydropyran-2-yl)hydroxylamine (0.049 g, 0.42 mmol) was added and the mixture was stirred at room temperature. After 30 minutes, LCMS showed complete conversion. Reaction was quenched by addition of water (5 mL) and the precipitate was filtered off, washed with water (2 mL) and hexane (5 mL) and dried to afford the title compound (0.055 g, 55%).

후처리

  1. stirringthe mixture was stirred at room temperature
  2. waitAfter 30 minutes
  3. customReaction
  4. customwas quenched by addition of water (5 mL)
  5. filtrationthe precipitate was filtered off
  6. washwashed with water (2 mL) and hexane (5 mL)
  7. customdried

출처 및 근거

ORD 기록
ord-6e2604004e0f4aaf82d86d57b695d067
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09029411B2

반응 노트

불러오는 중…