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Toluene → (2-Methylthiazol-4-yl)(7-oxa-3,10-diazaspiro[5.6]dodecan-10-yl)methanone trifluoroacetate

HRID 1689442
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HRID 1689442 반응식
[CH3:1][C:2]1[S:3][CH:4]=[C:5]([C:7]([N:9]2[CH2:27][CH2:26][C:13]3([CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]3)[O:12][CH2:11][CH2:10]2)=[O:8])[N:6]=1.[F:28][C:29]([F:34])([F:33])[C:30]([OH:32])=[O:31].C1(C)C=CC=CC=1>C(Cl)Cl>[F:28][C:29]([F:34])([F:33])[C:30]([OH:32])=[O:31].[CH3:1][C:2]1[S:3][CH:4]=[C:5]([C:7]([N:9]2[CH2:27][CH2:26][C:13]3([CH2:18][CH2:17][NH:16][CH2:15][CH2:14]3)[O:12][CH2:11][CH2:10]2)=[O:8])[N:6]=1
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 6422Trifluoroacetic acidHCID 57989321tert-Butyl 10-(2-methylthiazole-4-carbonyl)-7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate

생성물 1

HCID 67292347(2-Methylthiazol-4-yl)(7-oxa-3,10-diazaspiro[5.6]dodecan-10-yl)methanone trifluoroacetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of tert-butyl 10-(2-methylthiazole-4-carbonyl)-7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate (example 89, step f) (0.21 g) in DCM (10 mL) was treated with trifluoroacetic acid (10 mL) and the solution allowed to stand at 20° C. for 25 minutes. Toluene (40 mL) was added and the solvents evaporated under reduced pressure. The residue was azeotroped with acetonitrile to afford the subtitled compound. Yield 0.21 g.

후처리

  1. customthe solvents evaporated under reduced pressure
  2. customThe residue was azeotroped with acetonitrile

출처 및 근거

ORD 기록
ord-bc26712943da42b987af572a3ef0c2f6
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148373B2

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