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

Methanol → (S)-4-chloro-9-hydroxy-7,7-dimethyl-2',3',5',6,6',7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]-3-one

HRID 573791
ノート
印刷プレビュー

反応式

HRID 573791 の反応式
C1C2C(=CC=CC=2)[C@@H](N)[C@H]1O.B.CCN(C1C=CC=CC=1)CC.[Cl:24][C:25]1[C:34]2[C:35](=[O:43])[O:36][C:37]3([CH2:42][CH2:41][O:40][CH2:39][CH2:38]3)[C:33]=2[C:32]2[C:31](=[O:44])[CH2:30][C:29]([CH3:46])([CH3:45])[CH2:28][C:27]=2[N:26]=1.CO>O1CCCC1>[Cl:24][C:25]1[C:34]2[C:35](=[O:43])[O:36][C:37]3([CH2:42][CH2:41][O:40][CH2:39][CH2:38]3)[C:33]=2[C:32]2[C@@H:31]([OH:44])[CH2:30][C:29]([CH3:46])([CH3:45])[CH2:28][C:27]=2[N:26]=1
参加物反応条件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 887MethanolHCID 83312Diethylaniline-boraneHCID 2725045(1R,2S)-(+)-cis-1-Amino-2-indanol2 回HCID 866625334-chloro-7,7-dimethyl-2',3',5',6',7,8-hexahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]-3,9(6H)-dione

生成物 1

HCID 86662532(S)-4-chloro-9-hydroxy-7,7-dimethyl-2',3',5',6,6',7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]-3-one

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

213 mg (1R,2S)-(+)-cis-1-Amino-2-indanol are dissolved in 250 ml tetrahydrofurane and to this solution are dropwise added 3.58 ml of a borane-diethylaniline-complex. After completion of gas evolution the solution is cooled to 0° C. and 3.17 g 4-chloro-7,7-dimethyl-2′,3′,5′,6′,7,8-hexahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran]-3,9(6H)-dione in 250 ml tetrahydrofurane are added dropwise. The temperature is raised during 2 hours to room temperature and the mixture is stirred for 18 hours, 213 mg (1R,2S)-(+)-cis-1-Amino-2-indanol are added and stirring is continued for further 7 hours. 20 ml methanol are added dropwise and the mixture is stirred for additional 10 minutes. The mixture is partitioned between 0.1 M hydrochloric acid and ethylacetate. The aqueous phase is twice extracted with ethylacetate. The combined organic phases are dried with sodium sulphate and the solvents are evaporated in vacuo. The residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 0:100).

後処理

  1. temperatureThe temperature is raised during 2 hours to room temperature
  2. stirringstirring
  3. waitis continued for further 7 hours
  4. stirringthe mixture is stirred for additional 10 minutes
  5. customThe mixture is partitioned between 0.1 M hydrochloric acid and ethylacetate
  6. extractionThe aqueous phase is twice extracted with ethylacetate
  7. dry with materialThe combined organic phases are dried with sodium sulphate
  8. customthe solvents are evaporated in vacuo
  9. customThe residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 0:100)

出典と根拠

ORDレコード
ord-4d4d54b3d1504b99a543e1154d53dc7e
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029544B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート