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Dimethylformamide → HCID 68513610, 화합물

HRID 1947070
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HRID 1947070 반응식
[N:1]1([CH:7]2[CH2:11][NH:10][CH2:9][CH:8]2[OH:12])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[Cl:13][C:14]1[CH:22]=[CH:21][C:17]([C:18](Cl)=[O:19])=[CH:16][CH:15]=1.C(N([CH:29]([CH3:31])[CH3:30])CC)(C)C.CN([CH:35]=[O:36])C>CN(C1C=CN=CC=1)C>[Cl:13][C:14]1[CH:22]=[CH:21][C:17]([C:18]([N:4]2[CH2:3][CH2:2][N:1]([CH:7]3[CH:8]([OH:12])[CH2:9][N:10]([C:35]([C:30]4[CH:29]=[CH:31][C:14]([Cl:13])=[CH:15][CH:16]=4)=[O:36])[CH2:11]3)[CH2:6][CH2:5]2)=[O:19])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 85014-Chlorobenzoyl chlorideHCID 81531DiisopropylethylamineHCID 63701856HCID 63701856, 화합물

생성물 1

HCID 68513610HCID 68513610, 화합물

시약·촉매·용매 1

HCID 142844-(Dimethylamino)pyridine촉매

실험 절차

3,4-Epoxypyrrolidine carbamate Wang resin (0.15 g, 0.18 mmol) was placed in a glass reaction vessel (4 mL). LiClO4 (57 mg, 3 eq.), N-Boc piperazine (186 mg, 5.5 eq.) and acetonitrile (2 mL) were added. The glass reactor was closed with a screw cap and the reaction mixture was heated at 80° C. for 43 h. The resin was transferred into syringes and washed with acetonitrile:H2O (1:1, 2×), DMF (3×), MeOH (3×), DMF (3×), and CH2Cl2 (5×). The BOC group was removed by treating the resin with 10% methyl sulfide in TFA (2 mL) for 1 hour. This solution was saved and later combined with a cleavage solution. The product was further cleaved from resin by shaking with a solution of TFA:CH2Cl2:H2O (2 mL of 70:30:1.5) for 2.5 h (2×). All the solutions were combined and condensed to afford 170 mg of crude 4-piperazin-1-yl-pyrrolidin-3-ol (bistrifluoroacetate salt, used without purification). The crude 4-piperazin-1-yl-pyrrolidin-3-ol was dissolved in DMF (dry, 2 mL). To this solution was added 4-chloro-benzoyl chloride (46L, 0.36 mmol), diisopropyl ethyl amine (620 μL, 3.6 mmol), and DMAP (2 mg). The solution was stirred at RT for 30 minutes, and then separated by preparative LC-MS to yield 16 mg of the title compound as the trifluoroacetate salt. ESIMS ([M+H]+): 448.3 (100).

후처리

  1. customseparated by preparative LC-MS

출처 및 근거

ORD 기록
ord-465780c7f51848718174dab70355184e
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399455B2

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