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Isopropyl chloroformate → HCID 86629384, 화합물

HRID 1093298
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HRID 1093298 반응식
[Cl:1][C:2]1[N:7]=[C:6]2[N:8]([CH:11]3[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]3)[N:9]=[CH:10][C:5]2=[C:4]([N:17]2[CH2:23][CH:22]3[O:24][CH:19]([CH2:20][CH2:21]3)[CH2:18]2)[N:3]=1.C(N(CC)CC)C.Cl[C:33]([O:35][CH:36]([CH3:38])[CH3:37])=[O:34]>ClCCl.C1(C)C=CC=CC=1>[CH:22]12[O:24][CH:19]([CH2:20][CH2:21]1)[CH2:18][N:17]([C:4]1[N:3]=[C:2]([Cl:1])[N:7]=[C:6]3[N:8]([CH:11]4[CH2:12][CH2:13][N:14]([C:33]([O:35][CH:36]([CH3:38])[CH3:37])=[O:34])[CH2:15][CH2:16]4)[N:9]=[CH:10][C:5]=13)[CH2:23]2
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참가 물질

6

반응물 3

HCID 7917Isopropyl chloroformateHCID 8471TriethylamineHCID 86629385HCID 86629385, 화합물

생성물 1

HCID 86629384HCID 86629384, 화합물

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6344Dichloromethane용매2회

실험 절차

650 mg (1.7 mmol) of 3-(6-chloro-1-(piperidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane was suspended in 15 mL dichloromethane and triethylamine (0.5 mL) was added followed by addition of a 1N solution of isopropyl chloroformate in toluene. The mixture was stirred at room temperature overnight, diluted with dichloromethane and washed with sat. aqueous NaHCO3. The organic phase was dried over MgSO4, filtered and concentrated to give 696 mg (1.6 mmol) of the title compound. MS: 435.3/437.3 [M+H].

후처리

  1. washwashed with sat. aqueous NaHCO3
  2. dry with materialThe organic phase was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-281b82964f4844a6b2ebc2f3b2e08beb
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129371B2

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