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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tetrahydrofuran → 2-[(S)-1-{(3aS,7E,7aR)-7-(bromomethylene)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene-3-yl}ethoxy]-N-(2,2,3,3,3-pentafluoropropyl)acetamide

HRID 1922623
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HRID 1922623 반응식
C[Si](C)(C)[N-][Si](C)(C)C.[Na+].O1CCCC1.[Br:16]/[CH:17]=[C:18]1\[CH2:19][CH2:20][CH2:21][C@@:22]2([CH3:30])[C@H:26]\1[CH2:25][CH:24]=[C:23]2[C@@H:27]([OH:29])[CH3:28].Br[CH2:32][C:33]([NH:35][CH2:36][C:37]([F:43])([F:42])[C:38]([F:41])([F:40])[F:39])=[O:34].[Cl-].[NH4+]>CN(C)C=O.CCCCCC>[Br:16]/[CH:17]=[C:18]1\[CH2:19][CH2:20][CH2:21][C@@:22]2([CH3:30])[C@H:26]\1[CH2:25][CH:24]=[C:23]2[C@@H:27]([O:29][CH2:32][C:33]([NH:35][CH2:36][C:37]([F:42])([F:43])[C:38]([F:41])([F:39])[F:40])=[O:34])[CH3:28]
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참가 물질

8

반응물 5

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 2724254Sodium bis(trimethylsilyl)amideHCID 59456520(S)-1-{(3aS,7E,7aR)-7-(bromomethylene)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene-3-yl}ethanol2회HCID 594565462-bromo-N-(2,2,3,3,3-pentafluoropropyl)acetamide

생성물 1

HCID 24746036
2-[(S)-1-{(3aS,7E,7aR)-7-(bromomethylene)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene-3-yl}ethoxy]-N-(2,2,3,3,3-pentafluoropropyl)acetamide

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 8058Hexane용매

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온도
-15 °C

실험 절차

Under a nitrogen atmosphere, a solution of sodium hexamethyldisilazide in tetrahydrofuran (1.1 M, 5.31 ml, 5.84 mmol) was cooled to −15° C., and a solution of (S)-1-{(3aS,7E,7aR)-7-(bromomethylene)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene-3-yl}ethanol (Compound 5: 633.7 mg, 2.337 mmol) in dimethylformamide (1 ml) was added thereto over 4 minutes. The resulting mixture was stirred at −15° C. for 7 minutes, and a solution of 2-bromo-N-(2,2,3,3,3-pentafluoropropyl)acetamide (726 mg, 2.688 mmol) in dimethylformamide (1 ml) was added thereto over 5 minutes. After stirring the reaction solution at −5° C. for 30 minutes, aqueous ammonium chloride solution (5 ml) and hexane (20 ml) were added thereto, and the separation of the solution was conducted. The obtained organic layer was sequentially washed with water (5 ml) and saturated brine (4 ml)/water (1 ml), and the solvent was evaporated. The obtained crude product was purified by silica gel column chromatography to obtain 2-[(S)-1-{(3aS,7E,7aR)-7-(bromomethylene)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene-3-yl}ethoxy]-N-(2,2,3,3,3-pentafluoropropyl)acetamide (1.08 g, quantitatively).

후처리

  1. waitover 5 minutes
  2. stirringAfter stirring the reaction solution at −5° C. for 30 minutes
  3. customthe separation of the solution
  4. washThe obtained organic layer was sequentially washed with water (5 ml) and saturated brine (4 ml)/water (1 ml)
  5. customthe solvent was evaporated
  6. customThe obtained crude product
  7. customwas purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-89a0867db7f64800aea355d36476c984
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173824B2

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