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Diisopropylethylamine → HCID 70249298, 화합물

HRID 2088688
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HRID 2088688 반응식
[CH2:1]([O:3][C:4](=[O:30])[CH2:5][N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[N:20]=[C:19]3[N:14]([C:15](Cl)=[N:16][C:17]([C:21]4[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:22]=4[Cl:28])=[CH:18]3)[N:13]=2)[CH2:8][CH2:7]1)[CH3:2].Cl.[NH2:32][C:33]1[C:38]([C:39](=[O:44])[C:40]([F:43])([F:42])[F:41])=[CH:37][CH:36]=[C:35]([NH:45][CH2:46][CH2:47][NH2:48])[N:34]=1.C(N(CC)C(C)C)(C)C>CS(C)=O>[CH2:1]([O:3][C:4](=[O:30])[CH2:5][N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[N:20]=[C:19]3[N:14]([C:15]([NH:48][CH2:47][CH2:46][NH:45][C:35]4[CH:36]=[CH:37][C:38]([C:39](=[O:44])[C:40]([F:42])([F:43])[F:41])=[C:33]([NH2:32])[N:34]=4)=[N:16][C:17]([C:21]4[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:22]=4[Cl:28])=[CH:18]3)[N:13]=2)[CH2:8][CH2:7]1)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 58305987HCID 58305987, 화합물HCID 670603221-{2-Amino-6-[(2-aminoethyl)amino]pyridin-3-yl}-2,2,2-trifluoroethanone hydrochloride

생성물 1

HCID 70249298HCID 70249298, 화합물

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
130 °C

실험 절차

120 mg (0.23 mmol) of ethyl{4-[5-chlor-7-(2,4-dichlorophenyl)[1,2,4]triazolo[1,5-c]pyrimidin-2-yl]piperidin-1-yl}acetate (Example 55A), 78.7 mg (0.28 mmol) of 1-{2-amino-6-[(2-aminoethyl)-amino]pyridin-3-yl}-2,2,2-trifluoroethanone hydrochloride (Example 13A) and 0.24 ml (1.38 mmol) of N,N-diisopropylethylamine were initially charged in 1 ml of DMSO. The mixture was heated in the microwave at 130° C. for 30 min. This gave, after purification of the crude product by preparative HPLC (Method 11), 141 mg (90% of theory) of the product as a solid.

후처리

  1. customThis gave, after purification of the crude product by preparative HPLC (Method 11), 141 mg (90% of theory) of the product as a solid

출처 및 근거

ORD 기록
ord-155d1f1e0a5746eaa7b80d896f30fe25
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436003B2

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