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1-Hydroxybenzotriazole → 2-(4-Chloro-phenyl)-3-hydroxy-N-[5-(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-3-yl]-propionamide

HRID 82129
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HRID 82129 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:12][OH:13])[C:9]([OH:11])=O)=[CH:4][CH:3]=1.[NH2:14][C:15]1[CH:16]=[C:17]([C:21]([C:23]2[C:31]3[CH:30]=[N:29][CH:28]=[N:27][C:26]=3[N:25]([CH:32]([CH3:34])[CH3:33])[CH:24]=2)=[O:22])[CH:18]=[N:19][CH:20]=1.C(N(C(C)C)CC)(C)C.CCN=C=NCCCN(C)C.Cl.C1C=CC2N(O)N=NC=2C=1>C1COCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:12][OH:13])[C:9]([NH:14][C:15]2[CH:20]=[N:19][CH:18]=[C:17]([C:21]([C:23]3[C:31]4[CH:30]=[N:29][CH:28]=[N:27][C:26]=4[N:25]([CH:32]([CH3:34])[CH3:33])[CH:24]=3)=[O:22])[CH:16]=2)=[O:11])=[CH:6][CH:7]=1
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참가 물질

7

반응물 5

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 126063102-(4-Chlorophenyl)-3-hydroxypropanoic acidHCID 70817456(5-aminopyridin-3-yl)(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanone

생성물 1

HCID 70817680
2-(4-Chloro-phenyl)-3-hydroxy-N-[5-(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-3-yl]-propionamide
수율 3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
25 °C

실험 절차

2-(4-Chloro-phenyl)-3-hydroxy-propionic acid (570 mg, 2.84 mmol) (Preparation 244) was added to a solution of (5-Amino-pyridin-3-yl)-(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methanone (200 mg, 0.71 mmol) (Preparation 95) in THF (5 mL). Di-isopropyl ethylamine (0.64 mL, 3.56 mmol), EDCI.HCl (273 mg, 1.42 mmol) and HOBT (193 mg, 1.42 mmol) were added and the mixture was stirred at 25° C. for 48 hours. The reaction mixture was quenched with saturated aqueous sodium bicarbonate solution (2 mL) and extracted with ethyl acetate (3×15 mL). The combined organic layer was washed with water (5 mL), brine (5 mL), dried over sodium sulphate and evaporated in vacuo. The crude material was purified by preparative TLC (dichloromethane:methanol 93:7) to afford the title compound as a yellow solid in 3% yield, 10 mg.

후처리

  1. customThe reaction mixture was quenched with saturated aqueous sodium bicarbonate solution (2 mL)
  2. extractionextracted with ethyl acetate (3×15 mL)
  3. washThe combined organic layer was washed with water (5 mL), brine (5 mL)
  4. dry with materialdried over sodium sulphate
  5. customevaporated in vacuo
  6. customThe crude material was purified by preparative TLC (dichloromethane:methanol 93:7)

출처 및 근거

ORD 기록
ord-4d2638fba169438e86166e1822b0dc0d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846698B2

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