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3,4-Diaminopyridine → HCID 178525444, 화합물

HRID 266834
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HRID 266834 반응식
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:34]=[CH:33][C:13]([C:14]([N:16]2[CH2:21][CH2:20][CH:19]([N:22]3[C:32]4[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=4)[CH2:26][CH2:25][C:23]3=[O:24])[CH2:18][CH2:17]2)=[O:15])=[CH:12][CH:11]=1)([OH:3])=[O:2].[NH2:35][C:36]1[CH:37]=[N:38][CH:39]=[CH:40][C:41]=1[NH2:42].O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[CH3:57]S(O)(=O)=O.[OH-].[Na+]>>[NH:42]1[C:41]2[CH:40]=[CH:39][N:38]=[CH:37][C:36]=2[N:35]=[C:57]1[CH:4]([C:1]([OH:3])=[O:2])[CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:34]=[CH:33][C:13]([C:14]([N:16]2[CH2:17][CH2:18][CH:19]([N:22]3[C:32]4[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=4)[CH2:26][CH2:25][C:23]3=[O:24])[CH2:20][CH2:21]2)=[O:15])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

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6

반응물 5

HCID 59183,4-DiaminopyridineHCID 6395Methanesulfonic AcidHCID 14798Sodium HydroxideHCID 14812Phosphorus oxide (P4O10)HCID 190310461-{1-[4-(5-Carboxypentyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril

생성물 1

HCID 178525444HCID 178525444, 화합물

실험 절차

To 1-{1-[4-(5-carboxypentyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (2.00 g) are added 3,4-diaminopyridine (0.47 g), phosphorus pentoxide (1.00 g) and methanesulfonic acid (7.0 ml) and the mixture is stirred with heating at 100°-120° C. for 3 hours. After cooling, the reaction solution is poured into ice-water (30 ml) and the mixture is adjusted to around pH 11 with aqueous sodium hydroxide solution and extracted with dichloromethane. The extract is dried with magnesium sulfate and the solvent is distilled off. The resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=20:1→9:1) to give 1-{1-[4-(5-(imidazo[4,5-c]pyridine-2-yl)carboxypentyloxy)benzoyl]-4-piperidinyl]-3,4-dihydrocarbostyril (1.32 g) as white amorphous form.

후처리

  1. temperaturewith heating at 100°-120° C. for 3 hours
  2. temperatureAfter cooling
  3. extractionextracted with dichloromethane
  4. dry with materialThe extract is dried with magnesium sulfate
  5. distillationthe solvent is distilled off
  6. customThe resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=20:1→9:1)

출처 및 근거

ORD 기록
ord-435a73bbf412487a9679ff0200a53872
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05652247

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