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HCID 178463362, 화합물 → HCID 178463350, 화합물

HRID 81207
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HRID 81207 반응식
[Cl:1][C:2]1[C:7]([NH:8][CH:9]([C@H:11]2[CH2:16][CH2:15][C@H:14]([CH3:17])[CH2:13][CH2:12]2)[CH3:10])=[C:6]([NH:18]C(=O)OC(C)(C)C)[CH:5]=[C:4]([Cl:26])[N:3]=1>Cl.O1CCOCC1>[Cl:1][C:2]1[C:7]([NH:8][CH:9]([C@H:11]2[CH2:16][CH2:15][C@H:14]([CH3:17])[CH2:13][CH2:12]2)[CH3:10])=[C:6]([NH2:18])[CH:5]=[C:4]([Cl:26])[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 178463362HCID 178463362, 화합물

생성물 1

HCID 178463350HCID 178463350, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

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온도
50 °C

실험 절차

Crude tert-butyl (2,6-dichloro-3-((1-(trans-4-methylcyclohexyl)ethyl)amino)pyridin-4-yl)carbamate (70 g, 0.17 mol) was dissolved in a solution of HCl in dioxane (550 mL, 4 mol/L). The mixture was heated to 50° C. for 12 h. TLC (petroleum ether/ethyl acetate=5:1) showed the reaction was complete. White solid appeared. The solvent was removed under reduced pressure. The residue was washed with methyl tertiary butyl ether to give crude 2,6-dichloro-N3-(1-(trans-4-methylcyclohexyl)ethyl)pyridine-3,4-diamine, which was used for the next step without further purification. 1H NMR (400 MHz, DMSO-d6) δ: 6.63 (s, 1H), 3.16-3.13 (m, 1H), 1.84-1.76 (m, 2H), 1.67 (bs, 2H), 1.39 (bs, 1H), 1.25 (bs, 1H), 1.10-0.96 (m, 5H), 0.89-0.81 (m, 5H).

후처리

  1. customThe solvent was removed under reduced pressure
  2. washThe residue was washed with methyl tertiary butyl ether

출처 및 근거

ORD 기록
ord-dd5d5f61dc314b0683c88dfb9d7fa51a
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846657B2

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