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Indole-3-pyruvic acid → N-cyclohexyl 3-indolepyruvamide

HRID 359727
노트
인쇄 미리보기

반응식

HRID 359727 반응식
C[N-]C.[NH:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([CH2:13][C:14](=[O:18])[C:15]([OH:17])=O)=[CH:5]1.[CH:19]1[CH:20]=[CH:21][C:22]2N(O)N=[N:25][C:23]=2[CH:24]=1.C1(N)CCCCC1.CN1CCOCC1>CCN=C=NCCCN(C)C.Cl>[CH:23]1([NH:25][C:15](=[O:17])[C:14]([CH2:13][C:6]2[C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[NH:4][CH:5]=2)=[O:18])[CH2:24][CH2:19][CH2:20][CH2:21][CH2:22]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 803Indole-3-pyruvic acidHCID 7965CyclohexylamineHCID 79724-MethylmorpholineHCID 757711-HydroxybenzotriazoleHCID 182180Dimethylazanide

생성물 1

HCID 54134943N-cyclohexyl 3-indolepyruvamide

시약·촉매·용매 1

HCID 2723939
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
용매

실험 절차

The same method as described in Example 7 was followed for the preparation of N,N-dimethylamide. 500 mg 3-indolepyruvic acid were reacted with 400 ml HOBt and 570 ml EDC.HCl. 340 microliters of freshly distilled cyclohexylamine and 325 microliters NMM were added to the solution, which was reacted for 5 hours.

후처리

  1. customwas reacted for 5 hours

출처 및 근거

ORD 기록
ord-ab4f0216453f46f89472cb195305881f
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05002963

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