3-(Pyrrolidin-1-ylmethyl)thiomorpholine → 4-(6-Methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

HRID 1721643ノート

反応式

HRID 1721643 の反応式
[N:1]1([CH2:6][CH:7]2[CH2:12][S:11][CH2:10][CH2:9][NH:8]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19](=[O:27])[CH2:20][CH:21]2[C:24]([Cl:26])=[O:25])=[CH:17][CH:16]=1>C(N(CC)CC)C>[ClH:26].[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19](=[O:27])[CH2:20][CH:21]2[C:24]([N:8]2[CH2:9][CH2:10][S:11][CH2:12][CH:7]2[CH2:6][N:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)=[O:25])=[CH:17][CH:16]=1

参加物

4

反応物 2

HCID 157301473-(Pyrrolidin-1-ylmethyl)thiomorpholineHCID 189150696-Methoxy3-oxoindan-1-carbonyl chloride

生成物 1

HCID 189150334-(6-Methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride収率 42.1%

試薬・触媒・溶媒 1

HCID 8471Triethylamine溶媒

実験手順

The procedure described in Example 24 was repeated, but using 0.97 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.39 ml of triethylamine and 1.23 g of 6-methoxy-3-oxoindan-1-carbonyl chloride, to afford 0.9 g of the title compound, melting at 225°-233° C.

出典と根拠

ORDレコード
ord-e4283c09986b46a3bf039cf21c655a54
出典データセット
uspto-grants-1996_04
特許番号
US05512567

反応ノート

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