部分構造検索

21248

CCOC(=O)c1cc2ccc(Br)nc2[nH]1
Reaction #12006
desired product
収率 95.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2ccc(Br)nc2n1[C@H](C)CNC(=O)OC(C)(C)C
Reaction #12007
(R)-6-Bromo-1-(2-tert-butoxycarbonylamino-1-methyl-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNC(=O)c2cc3ccc(Br)nc3n21
Reaction #12008
(R)-6-Bromo-4-methyl-3,4-dihydro-2H-2,4a,5-triaza-fluoren-1-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(Br)nc3N21
Reaction #12009
(4R,9aR)-6-Bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@@H]2Cc3ccc(Br)nc3N21
Reaction #12010
(4R,9aS)-6-Bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc3n(c2n1)[C@H](C)CN(C(=O)OC(C)(C)C)C3
Reaction #12011
desired product
収率 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc2c(C)c(C)[nH]c2n1
Reaction #238801
DOI: 10.1039/C8SC04228D
CCn1c(C(=O)N(C2CC2)C2CC2)cc2c3c(ncn3C)c(Br)nc21
Reaction #273553
DOI: 10.1039/C8SC04228D
CCn1c(C(=O)N(C2CC2)C2CC2)cc2c3c(ncn3C)c(Br)nc21
Reaction #307579
4-Bromo-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(C(=O)N(C2CC2)C2CC2)cc2c3c(ncn3C)c(Nc3ccn(C)n3)nc21
Reaction #307580
N,N-Dicyclopropyl-6-ethyl-1-methyl-4-(1-methyl-1H-pyrazol-3-ylamino)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide
収率 29.5%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1-n1ccc2ccc(Br)nc21
Reaction #337869
2—(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2cc[nH]c2n1
Reaction #337870
6-bromo-1H-pyrrolo[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](C(C)C)(C(C)C)n1ccc2ccc(Br)nc21
Reaction #337871
6-bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Nc2ccc3cc[nH]c3n2)cc1
Reaction #337872
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1-n1ccc2ccc(Br)nc21
Reaction #340651
2—(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2cc[nH]c2n1
Reaction #340652
6-bromo-1H-pyrrolo[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(OCc5ccccc5)cc4=O)nc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562151
title compound
収率 33.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nc5)cc4=O)nc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562153
title compound
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562155
title compound
収率 24.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)cn5)cc4=O)nc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562157
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
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