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Diisopropylethylamine → HCID 57920212, 화합물

HRID 216041
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HRID 216041 반응식
Cl.[CH3:2][C:3]1([C:9]([NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]3[O:22][CH:21]=[N:20][CH:19]=3)[CH:13]=2)=[O:10])[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1.Cl[C:24]1[C:25]2[C:32]([CH3:33])=[CH:31][NH:30][C:26]=2[N:27]=[CH:28][N:29]=1.C(N(CC)C(C)C)(C)C>C(O)(C)C>[CH3:2][C:3]1([C:9]([NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]3[O:22][CH:21]=[N:20][CH:19]=3)[CH:13]=2)=[O:10])[CH2:4][CH2:5][N:6]([C:24]2[C:25]3[C:32]([CH3:33])=[CH:31][NH:30][C:26]=3[N:27]=[CH:28][N:29]=2)[CH2:7][CH2:8]1
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 148092824-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidineHCID 68993419HCID 68993419, 화합물

생성물 1

HCID 57920212HCID 57920212, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매

반응 조건

온도
105 °C

실험 절차

A pressure vessel was charged with a solution of 4-methyl-N-(3-(oxazol-5-yl)phenyl)piperidine-4-carboxamide hydrochloride from step B (51.9 mg, 0.17 mmol) and isopropanol (3 mL), and to this solution was added 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine (55.0 mg, 0.329 mmol) and N,N-diisopropylethylamine (297.9 mg, 0.40 mL, 2.31 mmol). The vessel was sealed, and the reaction was heated to 105° C. for 15 hours. The reaction was worked up by normal means, and the residue was purified by prep HPLC to afford the title compound as an off-white solid.

후처리

  1. customThe vessel was sealed
  2. customthe residue was purified by prep HPLC

출처 및 근거

ORD 기록
ord-4d775e918c2b4c3a9860be381b4a6b5e
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193202B2

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