Trifluoroacetic acid → HCID 22913027、化合物

HRID 2070093ノート

反応式

HRID 2070093 の反応式
[C:1]1([CH2:7][N:8]([CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:9]2[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][CH2:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)(C(F)(F)F)=O>ClCCl>[C:23]1([CH2:22][N:8]([CH2:7][C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

参加物

4

反応物 2

HCID 6422Trifluoroacetic acid2 回HCID 59444161HCID 59444161、化合物

生成物 1

HCID 22913027HCID 22913027、化合物収率 100%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

1,1-Dimethylethyl 4-[bis(phenylmethyl)amino]-1-piperidinecarboxylate D29 (160 g, 420 mmol) was dissolved in dichloromethane (DCM) (1 L) and TFA (188 mL, 2443 mmol) was added dropwise at room temperature. The resulting mixture was stirred for 3 h then further 100 mL of TFA was added and stirred for 2 h. The mixture was concentrated under reduced pressure and the residue treated with saturated solution NaHCO3 (1.5 L) and NaOH (3M solution; 200 mL) to basic pH. The aqueous phase was extracted with DCM (2×1.5 L). Combined organic layers were diluted with ethyl acetate (100 mL), washed with water (1×1 L) and brine (1×1 L) then dried on Na2SO4 and concentrated to obtain title material (118 g; 100%).

後処理

  1. stirringstirred for 2 h
  2. concentrationThe mixture was concentrated under reduced pressure
  3. additionthe residue treated with saturated solution NaHCO3 (1.5 L) and NaOH (3M solution; 200 mL) to basic pH
  4. extractionThe aqueous phase was extracted with DCM (2×1.5 L)
  5. additionCombined organic layers were diluted with ethyl acetate (100 mL)
  6. washwashed with water (1×1 L) and brine (1×1 L)
  7. customthen dried on Na2SO4
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-e75624edd61b4bc6b1e4261e6db2b700
出典データセット
uspto-grants-2012_10
特許番号
US08299257B2

反応ノート

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