Substructure Search

148163

Cc1nsc(NC(=O)Cc2ccc3oc(CC(C)(C)C)nc3c2)c1Cl
Reaction #76429
N-(4-chloro-3-methylisothiazol-5-yl)-[2-(2,2-dimethylpropyl)benzoxazol-5-yl]acetamide
Yield 28.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(=CN(C)C)c2ccc3oc(CC(C)(C)C)nc3c2)c1Cl
Reaction #76430
N-(4-chloro-3-methylisothiazol-5-yl)-α-[(dimethylamino)methylene]-[2-(2,2-dimethylpropyl)benzoxazol-5-yl]acetamide
Yield 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CCNC=C(C(=O)Nc1snc(C)c1Cl)c1ccc2oc(CC(C)(C)C)nc2c1
Reaction #76431
N-(4-chloro-3-methylisothiazol-5-yl)-α-[(ethylamino)methylene]-[2-(2,2-dimeth-ylpropyl)benzoxazol-5-yl]acetamide
Yield 85.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)c2ccc3oc(CC(C)(C)C)nc3c2)c1Cl
Reaction #76432
N-(4-chloro-3-methylisothiazol-5-yl)-2-[2-(2,2-dimethylpropyl)benzoxazol-5-yl]propionamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)C(=O)Nc2snc(C)c2Cl)cc1
Reaction #76436
N-(4-chloro-3-methylisothiazol-5-yl)-2-(4-methoxyphenyl)propionamide
Yield 89.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)c2ccc(O)cc2)c1Cl
Reaction #76437
N-(4-chloro-3-methylisothiazol-5-yl)-2-(4-hydroxyphenyl)propionamide
Yield 99.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)c2ccc(O)c(N)c2)c1Cl
Reaction #76438
N-(4-chloro-3-methylisothiazol-5-yl)-2-(3-amino-4-hydroxyphenyl)propionamide
Yield 89.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)c2ccc(O)c(NC(=O)CC(F)(F)F)c2)c1Cl
Reaction #76439
N-(4-chloro-3-methylisothiazol-5-yl)-2-[4-hydroxy-3-(3,3,3-trifluoropropionamido)phenyl]propionamide
Yield 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nsc(NC(=O)C(C)c2ccc3sc(CC(C)C)nc3c2)c1Cl
Reaction #76451
desired product
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)(F)c2ccc3oc(CC(C)(C)C)nc3c2)c1Cl
Reaction #76453
desired product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC(C)C)C(N)=O)ccc2C#N)sn1
Reaction #171987
(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-4-methylpentanamide
Yield 49.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](C)C(N)=O)ccc2C#N)sn1
Reaction #171990
(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)propanamide
Yield 61.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #171999
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172002
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC3CCCCC3)C(N)=O)ccc2C#N)sn1
Reaction #172007
(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-cyclohexylpropanamide
Yield 99.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172011
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@H](CC(C)C)C(N)=O)cc(F)c2C#N)sn1
Reaction #172013
(R)-2-(4-cyano-3-fluoro-5-(3-methylisothiazol-5-ylamino)phenylamino)-4-methylpentanamide
Yield 30.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172016
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(N[C@@H]3CCCC[C@@H]3N)c(F)cc2C(N)=O)sn1
Reaction #172018
titled compound
Yield 74.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2c(C(N)=O)ccc(N[C@H](CC(C)C)C(N)=O)c2F)sn1
Reaction #172020
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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