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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,5-Bis(trifluoromethyl)benzaldehyde → (S)-tert-butyl 5-(3,5-bistrifluoromethylbenzylamino)-7-methyl-8-trifluoromethyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate

HRID 507032
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HRID 507032 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1)[CH:6]=O.[NH2:17][C@H:18]1[CH2:24][CH2:23][CH2:22][N:21]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C:20]2[CH:32]=[C:33]([C:37]([F:40])([F:39])[F:38])[C:34]([CH3:36])=[CH:35][C:19]1=2.[BH4-].[Na+]>CO>[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1)[CH2:6][NH:17][C@H:18]1[CH2:24][CH2:23][CH2:22][N:21]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C:20]2[CH:32]=[C:33]([C:37]([F:40])([F:38])[F:39])[C:34]([CH3:36])=[CH:35][C:19]1=2
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참가 물질

5

반응물 3

HCID 1362473,5-Bis(trifluoromethyl)benzaldehydeHCID 4311764Sodium borohydrideHCID 59432516(S)-tert-Butyl 5-amino-7-methyl-8-(trifluoromethyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylate

생성물 1

HCID 59432291(S)-tert-butyl 5-(3,5-bistrifluoromethylbenzylamino)-7-methyl-8-trifluoromethyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate수율 98%

시약·촉매·용매 1

HCID 887
Methanol
용매

실험 절차

Add 3,5-bistrifluoromethylbenzaldehyde (909 mg, 3.75 mmol) to a solution of (S)-tert-butyl 5-amino-7-methyl-8-trifluoromethyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate (1.29 g, 3.75 mmol) in methanol (20 mL) at room temperature under nitrogen and stir for 2 h. Add sodium borohydride (283 mg, 7.5 mmol) and stir the mixture for 2 h. Remove the solvents under reduced pressure and dilute the residue with dichloromethane (50 mL) and water (50 mL). Collect the organic layer and extract the aqueous layer with dichloromethane (3×30 mL). Wash the combined organic extracts with water (20 mL) and brine (20 mL) and dry over anhydrous sodium sulfate. Filter and remove the solvents under reduced pressure to provide the title compound as an amber oil (2.09 g, 98%), which is used in the next step without purification. APCI MS m/z 570 (M+H)+.

후처리

  1. customRemove the solvents under reduced pressure
  2. additiondilute the residue with dichloromethane (50 mL) and water (50 mL)
  3. customCollect the organic layer
  4. extractionextract the aqueous layer with dichloromethane (3×30 mL)
  5. washWash the combined organic extracts with water (20 mL) and brine (20 mL)
  6. dry with materialdry over anhydrous sodium sulfate
  7. filtrationFilter
  8. customremove the solvents under reduced pressure

출처 및 근거

ORD 기록
ord-cfb940a52ba84f09ac3348de9cd58668
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786108B2

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