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3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-oxobutyric Acid → 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)indan-2-ylamino)acetylamino)-4-(4,6-dichlorobenzoxazol-2-yl)-4-oxobutyric Acid

HRID 1456663
ノート
印刷プレビュー

反応式

HRID 1456663 の反応式
[C:1]([NH:9][C@@H:10]([CH:45]([CH3:47])[CH3:46])[C:11]([N:13]([CH2:38][C:39]1C=[CH:43][CH:42]=[CH:41][CH:40]=1)[CH2:14][C:15]([NH:17][C@H](C(C1OC=C(C2C(Cl)=CC=CC=2Cl)N=1)=O)CC(O)=O)=[O:16])=[O:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:48](N[C@@H](C(C)C)C(N(CC(O)=O)CC1C=CC=CC=1)=O)(=O)[C:49]1C=CC=C[CH:50]=1.C(OC(=O)C(N)[C@H](C(OCC=C)=O)C(C1OC=C(C2C(Cl)=CC=CC=2Cl)N=1)O)(C)(C)C.C([O:110][C:111](=[O:134])[CH:112](N)[C@H:113](C(OCC=C)=O)[CH:114]([C:116]1[O:117][C:118]2[CH:124]=[C:123]([Cl:125])[CH:122]=[C:121]([Cl:126])[C:119]=2[N:120]=1)[OH:115])(C)(C)C.C(OC(=O)C[C@H](NC(=O)CN(C(=O)[C@@H](NC(=O)C1C=CC=CC=1)C(C)C)CC1C=CC=CC=1)C(C1OC=C(C2C(Cl)=CC=CC=2Cl)N=1)O)(C)(C)C>>[C:1]([NH:9][C@@H:10]([CH:45]([CH3:46])[CH3:47])[C:11]([N:13]([CH:38]1[CH2:50][C:49]2[C:40](=[CH:41][CH:42]=[CH:43][CH:48]=2)[CH2:39]1)[CH2:14][C:15]([NH:17][C@H:113]([C:114]([C:116]1[O:117][C:118]2[CH:124]=[C:123]([Cl:125])[CH:122]=[C:121]([Cl:126])[C:119]=2[N:120]=1)=[O:115])[CH2:112][C:111]([OH:110])=[O:134])=[O:16])=[O:12])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順出典と根拠反応ノート

参加物

6

反応物 5

HCID 536861393(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-oxobutyric AcidHCID 53859725((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetic AcidHCID 544408483(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-hydroxybutyric Acid tert-Butyl EsterHCID 697241953(S)-(Allyloxycarbonyl)-amino-4-((2,6-dichloro-phenyl)oxazol-2-yl)-4-hydroxy-butyric Acid tert-Butyl Ester
HCID 1317209653(S)-(Allyloxycarbonyl)-amino-4-(4,6-dichorobenzoxazol-2-yl)-4-hydroxy-butyric Acid tert-Butyl Ester

生成物 1

HCID 542387793(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)indan-2-ylamino)acetylamino)-4-(4,6-dichlorobenzoxazol-2-yl)-4-oxobutyric Acid

実験手順

Compound 725 was prepared by a method similar to the method used to prepare compound 710, except compound 704 was replaced with compound 724 and compound 707 was replaced with compound 718 in the preparation of compound 708: 1H NMR (500 MHz, CD3OD) δ 8.7-8.6 (m), 8.6-8.4 (m), 8.1 (d), 8.0-7.8 (m), 7.6-7.5 (m), 7.5-7.4 (m), 7.2-7.0 (m), 7.0-6.9 (m), 5.5-5.3 (m), 5.3-5.2 (m), 4.6-4.5 (m), 4.5-4.3 (m), 4.2-4.0 (m), 3.8-3.6 (m), 3.3 (s), 3.2-3.1 (m), 3.1-3.0 (m), 3.0-2.8 (m), 2.7-2.6 (m), 2.4-2.0 (m), 1.2-0.6 (m). ##STR104##

出典と根拠

ORDレコード
ord-5499f5eb6d314193a537298e38574ba3
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05843904

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出典と根拠反応ノート