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1,1-Dimethylethyl 4-[(2,6-dichloro-4-pyrimidinyl)amino]-1-piperidinecarboxylate → HCID 86618542, 화합물

HRID 2242969
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HRID 2242969 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]2[CH:20]=[C:19]([Cl:21])[N:18]=[C:17]([Cl:22])[N:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C>C(O)C.Cl.O1CCOCC1>[ClH:21].[ClH:21].[Cl:22][C:17]1[N:16]=[C:15]([NH:14][CH:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[CH:20]=[C:19]([Cl:21])[N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 866185411,1-Dimethylethyl 4-[(2,6-dichloro-4-pyrimidinyl)amino]-1-piperidinecarboxylate

생성물 1

HCID 86618542HCID 86618542, 화합물

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매HCID 312751,4-Dioxane용매

실험 절차

A solution of 4-(2,6-dichloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (3.1 g, 8.93 mmol) in ethanol (40 mL) and 4 M HCl in dioxane (70 mL) was stirred at rt for 2 h. The solvent was removed under reduced pressure and the crude product used in the consecutive step without further purification assuming quantitative deprotection and formation of the dihydrochloride salt. MS (ISP): 247.3 [M+H]+.

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후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe crude product used in the consecutive step without further purification

출처 및 근거

ORD 기록
ord-7a094e3c1c8d4e99bddad8e124611ed1
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07674804B2

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