1,1,3-trimethyl-2,3-dihydroinden-4-amine

CC1CC(C)(C)c2cccc(N)c21
Reaction #2465
desired product
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nnsc1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #250477
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nn(C)c(C)c1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #393212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CC(C)(C)c2cccc(NC(=O)c3cn(C)nc3C(F)(F)F)c21
Reaction #402850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012282
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012283
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012284
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012285
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012286
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012287
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012288
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012289
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1CC(C)(C)c2cccc(N)c21
Reaction #1012290
1,1,3-trimethyl-4-aminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1nn(C)c(C)c1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #1027198
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cc1ncsc1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #1119118
amorphous solid
Rendimiento 51.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
CC1CC(C)(C)c2cccc(NC(=O)c3nccnc3Cl)c21
Reaction #1119119
light yellow crystals
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
Cc1nnsc1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #1119120
white crystals
Rendimiento 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
Cc1occc1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #1119121
white crystals
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
CC1CC(C)(C)c2cccc(NC(=O)c3cn(C)nc3C(F)F)c21
Reaction #1292310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1nc(Cl)sc1C(=O)Nc1cccc2c1C(C)CC2(C)C
Reaction #1294620
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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