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Toluene → tert-Butyl (3S)-3-[({[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]amino}carbonyl)amino]pyrrolidine-1-carboxylate

HRID 541761
ノート
印刷プレビュー

反応式

HRID 541761 の反応式
C(Cl)(Cl)=O.C1(C)C=CC=CC=1.[NH2:12][C@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:14]1.C(N(CC)CC)C.FC(F)(F)[C:34]([OH:36])=O.FC(F)(F)C(O)=O.[Cl:46][C:47]1[CH:48]=[N:49][C:50]2[NH:51][C:52]3[CH:53]=[N:54][CH:55]=[C:56]([CH:69]=3)[CH2:57][CH2:58][C:59]3[CH:67]=[C:63]([NH:64][C:65]=1[N:66]=2)[CH:62]=[CH:61][C:60]=3[NH2:68]>C1COCC1>[Cl:46][C:47]1[CH:48]=[N:49][C:50]2[NH:51][C:52]3[CH:53]=[N:54][CH:55]=[C:56]([CH:69]=3)[CH2:57][CH2:58][C:59]3[CH:67]=[C:63]([NH:64][C:65]=1[N:66]=2)[CH:62]=[CH:61][C:60]=3[NH:68][C:34]([NH:12][C@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:14]1)=[O:36]
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 5

HCID 1140TolueneHCID 6371PhosgeneHCID 8471Triethylamine2 回HCID 854071tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 866361696-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-amine bis(trifluoroacetate)

生成物 1

HCID 57961783
tert-Butyl (3S)-3-[({[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]amino}carbonyl)amino]pyrrolidine-1-carboxylate
収率 61.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 20% phosgene in toluene (0.49 mL, 0.93 mmol) was added a solution of tert-butyl (3S)-3-aminopyrrolidine-1-carboxylate (38 mg, 0.20 mmol) and triethylamine (102 μL, 0.734 mmol) in THF (0.5 mL). The resulting solution was stirred for 2 hours then concentrated. To the isolated solids was added DCM (0.75 mL) followed by 6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-amine bis(trifluoroacetate) (70 mg, 0.1 mmol) and triethylamine (73 μL, 0.52 mmol). The resulting mixture was stirred at room temperature overnight and concentrated. The residue was purified by flash column chromatography to yield the desired product (34 mg, 50%). LCMS calculated for C27H32ClN8O3(M+H)+: m/z=551.1.

後処理

  1. concentrationthen concentrated
  2. additionTo the isolated solids was added DCM (0.75 mL)
  3. stirringThe resulting mixture was stirred at room temperature overnight
  4. concentrationconcentrated
  5. customThe residue was purified by flash column chromatography

出典と根拠

ORDレコード
ord-e573a85c93f941d7bb6052b86e4ce5ae
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871753B2

反応ノート

読み込み中…

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