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Diisopropylethylamine → HCID 86660190, 화합물

HRID 2368320
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인쇄 미리보기

반응식

HRID 2368320 반응식
[NH2:1][C:2]1[C:3]([C:8]([OH:10])=O)=[N:4][CH:5]=[N:6][CH:7]=1.[NH2:11][CH2:12][C:13]([CH3:16])([OH:15])[CH3:14].C(N(C(C)C)C(C)C)C.CCCP1(OP(CCC)(=O)OP(CCC)(=O)O1)=O>C1COCC1>[OH:15][C:13]([CH3:16])([CH3:14])[CH2:12][NH:11][C:8]([C:3]1[C:2]([NH2:1])=[CH:7][N:6]=[CH:5][N:4]=1)=[O:10]
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참가 물질

6

반응물 4

HCID 81531DiisopropylethylamineHCID 951022-Propanol, 1-amino-2-methyl-HCID 111923Propylphosphonic anhydrideHCID 122589125-Aminopyrimidine-4-carboxylic acid

생성물 1

HCID 86660190HCID 86660190, 화합물수율 72%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

To a stirred mixture of 5-aminopyrimidine-4-carboxylic acid (200 mg, 1.44 mmol) and 1-amino-2-methylpropan-2-ol (128 mg, 1.44 mmol) at rt in THF (5 ml) under an argon atmosphere were added N-ethyldiisoproplyamine (743 mg, 978 μl, 5.75 mmol) and 1-propanephosphonic acid cyclic anhydride (2.29 g, 2.16 ml, 3.59 mmol). The mixture was stirred at rt for 21 hrs, then concentrated. The crude product was purified by column chromatography with EtOAc/MeOH as eluent providing the title compound (216 mg, 72%) as off-white solid.

후처리

  1. concentrationconcentrated
  2. customThe crude product was purified by column chromatography with EtOAc/MeOH as eluent

출처 및 근거

ORD 기록
ord-b6011126272c4141a351e13c659aa1d8
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703768B2

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