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Diisopropylethylamine → HCID 11446836、化合物

HRID 2038899
ノート
印刷プレビュー

反応式

HRID 2038899 の反応式
Cl.[NH:2]1[C@H:6]([C:7]([O:9]CC2C=CC=CC=2)=[O:8])[CH2:5][C@@H:4]2[CH2:17][CH2:18][CH2:19][C@H:3]12.C(OC(OC(C)(C)C)=O)(OC(C)(C)C)=O.C(N(CC)C(C)C)(C)C>C(Cl)Cl.CN(C)C1C=CN=CC=1>[NH:2]1[CH:6]([C:7]([OH:9])=[O:8])[CH2:5][CH:4]2[CH2:17][CH2:18][CH2:19][CH:3]12
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 81531DiisopropylethylamineHCID 90495Di-tert-butyl dicarbonateHCID 13216857Cyclopenta(b)pyrrole-2-carboxylic acid, octahydro-, phenylmethyl ester, hydrochloride (1:1), (2S,3aS,6aS)-

生成物 1

HCID 11446836HCID 11446836、化合物

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒
HCID 6344
Dichloromethane
溶媒

実験手順

To a solution of commercially available (2S,3aS,6aS)-benzyl octahydrocyclopenta[b]pyrrole-2-carboxylate hydrochloride (4.70 g, 16.68 mmol) in methylene chloride (42 mL) was added Di-tert-butyl dicarbonate (7.28 g, 33.36 mmol), N,N-diisopropylethylamine (5.82 mL, 33.36 mmol) and 4-(Dimethylamino)pyridine (0.20 g, 1.67 mmol). The solution was stirred under air for 16 hours. Upon completion, the reaction was concentrated in vacuo, diluted in ethyl acetate, and washed with 1N HCl. The aqueous layers were backextracted twice with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated. The resulting residue was purified by silica gel chromatography (5-40% ethyl acetate in hexanes) to afford (2S,3aS,6aS)-1-tert-butoxycarbonyl)octahydrocyclopenta[b]pyrrole-2-carboxylic acid which was used without further purification. MS (ESI) m/z 368.47 [M+Na]+.

後処理

  1. concentrationUpon completion, the reaction was concentrated in vacuo
  2. additiondiluted in ethyl acetate
  3. washwashed with 1N HCl
  4. dry with materialthe combined organic layers were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe resulting residue was purified by silica gel chromatography (5-40% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-7d7172a291c54c55940be3820faad7cf
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08575135B2

反応ノート

読み込み中…

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