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(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid dimethylamide → (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acid

HRID 377077
ノート
印刷プレビュー

反応式

HRID 377077 の反応式
C[N:2]([CH3:20])[C:3]([C:5]1[C@H:6]2[CH2:18][C@@H:17]3O[C@@H:16]3[C@@H:7]2[C@H:8](OC(=O)NC)OC=1)=[O:4].[CH3:21][N:22](C)[C:23]([C:25]1[C@H:26]2[CH2:38][C@@H:37]3[O:39][C@:36]3([CH3:40])[C@@H:27]2[C@H:28]([O:31][C:32](=[O:35])[NH:33][CH3:34])[O:29][CH:30]=1)=[O:24]>>[N:2]1([NH:22][C:23]([C:25]2[C@H:26]3[CH2:38][C@@H:37]4[O:39][C@:36]4([CH3:40])[C@@H:27]3[C@H:28]([O:31][C:32](=[O:35])[NH:33][CH3:34])[O:29][CH:30]=2)=[O:24])[CH2:3][CH2:5][CH2:6][CH2:20]1.[CH2:21]([NH:22][C:23]([C:25]1[C@H:26]2[CH2:38][C@@H:37]3[O:39][C@:36]3([CH3:40])[C@@H:27]2[C@H:28]([O:31][C:32](=[O:35])[NH:33][CH3:34])[O:29][CH:30]=1)=[O:24])[C:8]1[CH:7]=[CH:16][CH:17]=[CH:18][CH:6]=1.[O:39]1[C@@:36]2([CH3:40])[C@@H:37]1[CH2:38][C@@H:26]1[C:25]([C:23]([OH:4])=[O:24])=[CH:30][O:29][C@@H:28]([O:31][C:32](=[O:35])[NH:33][CH3:34])[C@H:27]12
参加物実験手順出典と根拠反応ノート

参加物

5

反応物 2

HCID 57301816(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid dimethylamideHCID 86755116(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid dimethylamide

生成物 3

HCID 18397301(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acid
HCID 57159362
(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acid benzylamide
HCID 86755115(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid pyrrolidylamide

実験手順

(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid dimethylamide (Table 4, Compound No. 18), (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid dimethylamide (Table 4, Compound No. 19), (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid pyrrolidylamide (Table 5, Compound No. 25), and (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid benzylamide (Table 6, Compound No. 27) were produced in the same manner from (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy)cyclopenta[c]-pyrane-4-carboxylic acid. The physicochemical properties of the above compounds are described in the attached tables (corresponding to Table No. and Compound No.).

出典と根拠

ORDレコード
ord-2259bbabfe7b4905ad13debd3288562a
出典データセット
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06022888

反応ノート

読み込み中…

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