ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Citric Acid → 4-(tert-Butyl-dimethyl-silanyloxy)-3-({6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carbonyl}-amino)-butyric acid

HRID 1824443
ノート
印刷プレビュー

反応式

HRID 1824443 の反応式
C([O:8][C:9](=[O:49])[CH2:10][CH:11]([NH:21][C:22]([CH:24]1[N:28]2[C:29](=[O:48])[CH:30]([NH:35][C:36]([C:38]3[CH:47]=[CH:46][C:45]4[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=4)[CH:39]=3)=[O:37])[CH2:31][CH:32]=[CH:33][CH2:34][CH:27]2[CH2:26][CH2:25]1)=[O:23])[CH2:12][O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])C1C=CC=CC=1.[OH-].[Na+].O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[C:17]([Si:14]([CH3:16])([CH3:15])[O:13][CH2:12][CH:11]([NH:21][C:22]([CH:24]1[N:28]2[C:29](=[O:48])[CH:30]([NH:35][C:36]([C:38]3[CH:47]=[CH:46][C:45]4[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=4)[CH:39]=3)=[O:37])[CH2:31][CH:32]=[CH:33][CH2:34][CH:27]2[CH2:26][CH2:25]1)=[O:23])[CH2:10][C:9]([OH:49])=[O:8])([CH3:19])([CH3:18])[CH3:20]
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 4

HCID 311Citric AcidHCID 962WaterHCID 14798Sodium HydroxideHCID 695844714-(tert-Butyl-dimethyl-silanyloxy)-3-({6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carbonyl}-amino)-butyric acid benzyl ester

生成物 1

HCID 69584478
4-(tert-Butyl-dimethyl-silanyloxy)-3-({6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carbonyl}-amino)-butyric acid
収率 96.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution containing 4-(tert-Butyl-dimethyl-silanyloxy)-3-({6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carbonyl}-amino)-butyric acid benzyl ester (590 mg, 0.86 mmol) in MeOH (10 mL) is treated with 1N NaOH (2.5 mL) and stirred at rt for 12 hrs. The solution was poured into water, acidified to pH=3 with 10% citric acid, and extracted with EtOAc. The combined organic extracts are washed with brine and dried over Na2SO4. The solution is filtered and concentrated to yield 492 mg of desired product that was used without further purification. MS (ESI) 594 (M+1).

後処理

  1. extractionextracted with EtOAc
  2. washThe combined organic extracts are washed with brine
  3. dry with materialdried over Na2SO4
  4. filtrationThe solution is filtered
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-5d0b422ed0cc44b394ac1a6d0a480269
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07041696B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート