Hydrochloric Acid → (1S,2R,3S,4S,5R,6R)-2-Amino-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid hydrochloride

HRID 2173011ノート

反応式

HRID 2173011 の反応式
O.Cl.C(OC([NH:10][C@@:11]1([C:35]([O:37]C(C)(C)C)=[O:36])[C@H:16]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[C:21]([Cl:26])[CH:20]=2)[C@@H:15]([OH:27])[C@@H:14]2[C@H:12]1[C@H:13]2[C:28]([O:30]C(C)(C)C)=[O:29])=O)(C)(C)C>O1CCOCC1>[ClH:25].[NH2:10][C@@:11]1([C:35]([OH:37])=[O:36])[C@H:16]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[C:21]([Cl:26])[CH:20]=2)[C@@H:15]([OH:27])[C@@H:14]2[C@H:12]1[C@H:13]2[C:28]([OH:30])=[O:29]

参加物

5

反応条件

温度
100 °C

実験手順

A mixture of water (430 mL) and 37% HCl in water (299.9 mL, 3.65 mol) is added to a suspension of di-tert-butyl (1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate (215 g, 365.3 mmol) in 1,4-dioxane (73.1 mL). The resulting slurry is stirred at 100° C. for 4.5 hours, cooled to 25° C. and concentrated in vacuo to provide a white solid. Triturate sequentially with methyl tert-butyl ether (2 L) and hexanes (2 L) and then filter to collect the solids. Dry under vacuum for 16 hours. The solid is washed again with methyl tert-butyl ether (2×1 L) and hexane (1 L), then dried under vacuum at 50° C. overnight to yield the title compound as a white solid (140.4 g, 93% yield). MS (m/z): 376/378 (M+1).

後処理

  1. temperaturecooled to 25° C.
  2. concentrationconcentrated in vacuo
  3. customto provide a white solid
  4. customTriturate sequentially with methyl tert-butyl ether (2 L) and hexanes (2 L)
  5. filtrationfilter
  6. customto collect the solids
  7. customDry under vacuum for 16 hours
  8. washThe solid is washed again with methyl tert-butyl ether (2×1 L) and hexane (1 L)
  9. customdried under vacuum at 50° C. overnight

出典と根拠

ORDレコード
ord-a28f5427f1d349e7b2fbc16c997171dc
出典データセット
uspto-grants-2015_06
特許番号
US09056844B2

反応ノート

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