Ammonium Chloride → 5-{[6-(2-Hydroxy-1-morpholin-4-ylethyl)pyridin-2-yl]amino}-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxamide

HRID 2060635노트

반응식

HRID 2060635 반응식
[OH:1][CH2:2][CH:3]([C:10]1[N:15]=[C:14]([NH:16][C:17]2[S:21][C:20]([C:22]3[CH:23]=[N:24][C:25]([N:28]4[CH2:33][CH2:32][O:31][CH2:30][CH2:29]4)=[CH:26][CH:27]=3)=[N:19][C:18]=2[C:34]([OH:36])=O)[CH:13]=[CH:12][CH:11]=1)[N:4]1[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1.O[N:38]1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.[Cl-].[NH4+].C(N(C(C)C)CC)(C)C>CN(C=O)C.O>[OH:1][CH2:2][CH:3]([C:10]1[N:15]=[C:14]([NH:16][C:17]2[S:21][C:20]([C:22]3[CH:23]=[N:24][C:25]([N:28]4[CH2:33][CH2:32][O:31][CH2:30][CH2:29]4)=[CH:26][CH:27]=3)=[N:19][C:18]=2[C:34]([NH2:38])=[O:36])[CH:13]=[CH:12][CH:11]=1)[N:4]1[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1

참가 물질

8

실험 절차

5-{[6-(2-Hydroxy-1-morpholin-4-ylethyl)pyridin-2-yl]amino}-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxylic acid (64 mg, 0.13 mmol), N-hydroxybenzotriazole (39 mg, 0.25 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (48 mg, 0.25 mmol), and ammonium chloride (34 mg, 0.63 mmol) were taken up in DMF (4.2 mL) under argon. Diisopropylethylamine (110 μl, 0.63 mmol) was added and the mixture was stirred at room temperature for 36 hours. The solution was then diluted with water to precipitate a white solid that was collected by filtration, washed with water and dried under reduced pressure to afford the title compound as a bright yellow solid. 1H NMR (500 MHz, d6-DMSO): δ 11.21 (s, 1H), 8.66 (d, 1H), 8.08 (dd, 1H), 7.72 (s, 1H), 7.69 (t, 1H), 7.59 (s, 1H), 7.05 (d, 1H), 6.96 (d, 1H), 6.93 (d, 1H), 4.53 (m, 1H), 3.99 (m, 2H), 3.69 (m, 5H), 3.55 (m, 8H), 2.50 (m, 4H). LRMS (APCI) calc'd for C24H30N7O4S [M+H]+ 512.2, found 512.1

후처리

  1. customto precipitate a white solid
  2. filtrationthat was collected by filtration
  3. washwashed with water
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-f8726849af1e49c8b287f8605402c63f
출처 데이터셋
uspto-grants-2012_10
특허 번호
US08278335B2

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