反応 #2290316

ord-47a170b932204ece87c5c88b09c8970c

反応方程式

N[C@H](C(=O)O)C1CCOCC1
(S)-amino-(tetrahydro-pyran-4-yl)-acetic acid
O=C([O-])O.[Na+]
sodium bicarbonate
COC(=O)Cl
Methyl chloroformate
COC(=O)N[C@H](C(=O)O)C1CCOCC1
title intermediate
収率 99.7%
COC(=O)N[C@H](C(=O)O)C1CCOCC1
(S)-Methoxycarbonylamino-(tetrahydro-pyran-4-yl)-acetic acid
収率 99.7%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.DISSOLUTIONwere dissolved
  2. 2
    抽出The reaction mixture was extracted with ethyl acetate (3×15 mL)
  3. 3
    乾燥the organic extracts were dried over sodium sulfate
  4. 4
    ろ過filtered
  5. 5
    濃縮concentrated
  6. 6
    その他dried overnight under vacuum

実験手順

A solution of (S)-amino-(tetrahydro-pyran-4-yl)-acetic acid (1 g, 6.28 mmol) in saturated aqueous sodium bicarbonate solution (12.32 mL, 125.6 mmol) was stirred until all solids were dissolved. Methyl chloroformate (0.97 mL, 12.56 mmol) was added dropwise, the reaction mixture was stirred for 1 h, and IN HCl was added to adjust pH to 1. The reaction mixture was extracted with ethyl acetate (3×15 mL) and the organic extracts were dried over sodium sulfate, filtered, concentrated and dried overnight under vacuum to give the title intermediate (1.36 g, 99% yield) as a white, sticky solid. (m/z): [M+H]+ calcd for C9H15NO5 218.10 found 218.3.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09365549B2uspto-grants-2016_06