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2-Aminothiazole → 4-[(3R,3'S)-3-(3,5-Dichlorophenyl)-2'-oxo-1,3'-bipyrrolidin-1'-yl]-N-(thiazol-2-yl)benzenesulfonamide

HRID 2261481
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HRID 2261481 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.C(N=C(N(C)C)N(C)C)(C)(C)C.[Cl:19][C:20]1[CH:21]=[C:22]([C@H:27]2[CH2:31][CH2:30][N:29]([C@H:32]3[CH2:36][CH2:35][N:34]([C:37]4[CH:42]=[CH:41][C:40]([S:43](Cl)(=[O:45])=[O:44])=[CH:39][CH:38]=4)[C:33]3=[O:47])[CH2:28]2)[CH:23]=[C:24]([Cl:26])[CH:25]=1>C(#N)C>[Cl:26][C:24]1[CH:23]=[C:22]([C@H:27]2[CH2:31][CH2:30][N:29]([C@H:32]3[CH2:36][CH2:35][N:34]([C:37]4[CH:38]=[CH:39][C:40]([S:43]([NH:1][C:2]5[S:3][CH:4]=[CH:5][N:6]=5)(=[O:44])=[O:45])=[CH:41][CH:42]=4)[C:33]3=[O:47])[CH2:28]2)[CH:21]=[C:20]([Cl:19])[CH:25]=1
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참가 물질

5

반응물 3

HCID 21552-AminothiazoleHCID 35715812-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 866377574-[(3R,3'S)-3-(3,5-dichlorophenyl)-2'-oxo-1,3'-bipyrrolidin-1'-yl]benzene-1-sulfonyl chloride

생성물 1

HCID 446034274-[(3R,3'S)-3-(3,5-Dichlorophenyl)-2'-oxo-1,3'-bipyrrolidin-1'-yl]-N-(thiazol-2-yl)benzenesulfonamide수율 29.5%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매
2회

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온도
0 °C

실험 절차

Synthesized according to General Procedure 12, Method B: To a stirred solution of 2-aminothiazole (88.8 mg, 0.89 mmol) in acetonitrile (1 ML) at 0° C. was added 2-tert-butyl-1,1,3,3-tetramethylguanidine (152 mg, 0.89 mmol) dropwise and the reaction mixture was stirred at 0° C. for 15 min. To this was slowly added a suspension of 4-[(3R,3′S)-3-(3,5-dichlorophenyl)-2′-oxo-1,3′-bipyrrolidin-1′-yl]benzene-1-sulfonyl chloride (100 mg, 0.17 mmol) in acetonitrile (0.5 mL) and the reaction mixture was stirred at 0° C. for 15 min, the cooling bath was removed and the reaction mixture was stirred at RT for 30 min. The reaction mixture was then poured into water, the pH was adjusted to ˜7 with 1M HCl, and extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated to dryness. Purification by silica gel chromatography (0-10% MeOH in EtOAc) afforded the desired product as a solid (27 mg, 28%). 1H-NMR (400 MHz, DMSO-d6) δ 7.84-7.77 (m, 4H), 7.43-7.37 (m, 3H), 7.24 (d, J=4.6 Hz, 1H), 6.81 (d, J=4.6 Hz, 1H), 3.83-3.72 (m, 2H), 3.58 (t, J=8.8 Hz, 1H), 3.07-2.96 (m, 3H), 2.87 (td, J=8.6, 4.3 Hz, 1H), 2.34-2.20 (m, 2H), 2.11-2.02 (m, 1H) and 1.74 (dt, J=19.9, 6.9 Hz, 1H) ppm. LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=537.3; tR=1.21 min.

후처리

  1. customSynthesized
  2. additionTo this was slowly added
  3. stirringthe reaction mixture was stirred at 0° C. for 15 min
  4. customthe cooling bath was removed
  5. stirringthe reaction mixture was stirred at RT for 30 min
  6. additionThe reaction mixture was then poured into water
  7. extractionextracted with EtOAc (3×)
  8. washThe combined organic extracts were washed with brine
  9. dry with materialdried over Na2SO4
  10. customevaporated to dryness
  11. customPurification by silica gel chromatography (0-10% MeOH in EtOAc)

출처 및 근거

ORD 기록
ord-d38dae9b0b664e3ebd43357a77ee4057
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846954B2

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