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Phosgene → HCID 15053374、化合物

HRID 974572
ノート
印刷プレビュー

反応式

HRID 974572 の反応式
C(=O)([O-])[O-].[K+].[K+].C(Cl)(Cl)=[O:8].C1([CH:17]([N:19]2[CH2:22][CH:21]([O:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=3)[CH2:20]2)C)C=CC=CC=1.[CH2:30]([NH2:33])[CH:31]=[CH2:32]>C(Cl)Cl.C1C=CC=CC=1>[CH2:30]([NH:33][C:17]([N:19]1[CH2:20][CH:21]([O:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[CH2:22]1)=[O:8])[CH:31]=[CH2:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6371PhosgeneHCID 7853AllylamineHCID 11430Potassium CarbonateHCID 15053368HCID 15053368、化合物

生成物 1

HCID 15053374HCID 15053374、化合物

試薬・触媒・溶媒 2

HCID 241Benzene溶媒HCID 6344
Dichloromethane
溶媒
2 回

実験手順

To a stirred suspension of 10 g (0.072 mole) of finely ground potassium carbonate in 90 ml of methylene chloride was added 32 ml (0.062 mole) of 2M of phosgene in benzene. The mixture was stirred for 15 min and 8 g (0.031 mole) of 1-(1-phenylethyl)-3-(2-pyridyloxy)azetidine in 50 ml of methylene chloride was added. The mixture was stirred at 25° C. for 2 hr and concentrated on a rotary evaporator at 25° C./30 mm and the residue was treated with 100 ml of tetrahydrofuran. The stirred mixture was cooled with an ice bath and treated dropwise with 4 g (0.07 mole) of allyl amine. After stirring 30 min at 25° C., the material was partitioned between water and methylene chloride. The methylene chloride was dried and concentrated. The residue was chromatographed on a Waters® PREP-500 HPLC using a silica column and eluting with 50% ethylacetate-hexane. The product was crystallized twice from isopropyl ether. Yield of title compound was 1.5 g (21%), m.p. 72°-76° C.

後処理

  1. stirringThe mixture was stirred at 25° C. for 2 hr
  2. concentrationconcentrated on a rotary evaporator at 25° C./30 mm
  3. additionthe residue was treated with 100 ml of tetrahydrofuran
  4. temperatureThe stirred mixture was cooled with an ice bath
  5. stirringAfter stirring 30 min at 25° C.
  6. customthe material was partitioned between water and methylene chloride
  7. dry with materialThe methylene chloride was dried
  8. concentrationconcentrated
  9. customThe residue was chromatographed on a Waters®
  10. washeluting with 50% ethylacetate-hexane
  11. customThe product was crystallized twice from isopropyl ether

出典と根拠

ORDレコード
ord-34bfdb1bb37c4850ae40ecdb007e5a5f
出典データセット
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05068231

反応ノート

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