5-Aminopentan-1-ol → 3-(2-Chloro-4-iodo-phenylamino)-N-(5-hydroxy-pentyl)-isonicotinamide

HRID 39542

반응식

HRID 39542 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=O.[NH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][OH:25]>>[Cl:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([NH:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][OH:25])=[O:14]

참가 물질

3

반응물 2

HCID 756345-Aminopentan-1-olHCID 576496513-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid2회

생성물 1

HCID 117122943-(2-Chloro-4-iodo-phenylamino)-N-(5-hydroxy-pentyl)-isonicotinamide

실험 절차

3-(2-Chloro-4-iodo-phenylamino)-N-(5-hydroxy-pentyl)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.30 mmol of 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid (intermediate 2) and 0.40 mmol of 5-amino-pentan-1-ol. LC/MS [9.33 min; 461 (M+1)]

후처리

  1. customLC/MS [9.33 min; 461 (M+1)]

출처 및 근거

ORD 기록
ord-be706f19a49f4a5493ee98443921e539
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524911B2

연결된 노트

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